Linked Data
dbSNP Id:
rs1199052957
gnomAD v2:
12-6702267-T-C
gnomAD v3:
12-6593101-T-C
gnomAD v4:
12-6593101-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6593101T>C , CM000674.2:g.6593101T>C | GRCh38 |
| NC_000012.11:g.6702267T>C , CM000674.1:g.6702267T>C | GRCh37 |
| NC_000012.10:g.6572528T>C | NCBI36 |
| NG_052823.1:g.19339A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357008.7:c.2603A>G | ENSP00000349508.3:p.Asn868Ser | |
| ENST00000544040.7:c.2642A>G MANE Select | ENSP00000440542.2:p.Asn881Ser | |
| ENST00000544484.6:c.2633A>G | ENSP00000440392.1:p.Asn878Ser | |
| ENST00000642594.1:c.2568A>G | ||
| ENST00000642810.1:c.2582A>G | ENSP00000495160.1:p.Asn861Ser | |
| ENST00000642879.1:c.2582A>G | ENSP00000494456.1:p.Asn861Ser | |
| ENST00000643335.1:c.2621A>G | ENSP00000496358.1:p.Asn874Ser | |
| ENST00000643815.1:c.1359A>G | ||
| ENST00000644137.1:c.2621A>G | ENSP00000495816.1:p.Asn874Ser | |
| ENST00000644289.1:c.2609A>G | ENSP00000496707.1:p.Asn870Ser | |
| ENST00000644352.1:c.500A>G | ENSP00000494981.1:p.Asn167Ser | |
| ENST00000644356.1:n.597A>G | ||
| ENST00000644480.2:c.2621A>G | ENSP00000493629.2:p.Asn874Ser | |
| ENST00000644801.1:c.2621A>G | ENSP00000496660.1:p.Asn874Ser | |
| ENST00000645005.1:c.2642A>G | ENSP00000493471.1:p.Asn881Ser | |
| ENST00000645022.1:c.2621A>G | ENSP00000496163.1:p.Asn874Ser | |
| ENST00000645095.1:c.2642A>G | ENSP00000496634.1:p.Asn881Ser | |
| ENST00000645645.1:c.2603A>G | ENSP00000496543.1:p.Asn868Ser | |
| ENST00000646268.1:c.2621A>G | ENSP00000495023.1:p.Asn874Ser | |
| ENST00000646366.1:n.2222A>G | ||
| ENST00000646608.1:c.1570A>G | ||
| ENST00000646806.1:c.2582A>G | ENSP00000494574.1:p.Asn861Ser | |
| ENST00000647483.1:c.643A>G | ||
| ENST00000357008.6:c.2642A>G | ENSP00000349508.2:p.Asn881Ser | |
| ENST00000544040.5:c.2621A>G | ENSP00000440542.1:p.Asn874Ser | |
| ENST00000544484.5:c.2633A>G | ENSP00000440392.1:p.Asn878Ser | |
| NM_001273.3:c.2642A>G | NP_001264.2:p.Asn881Ser | |
| NM_001297553.1:c.2621A>G | NP_001284482.1:p.Asn874Ser | |
| XM_005253668.3:c.2621A>G | XP_005253725.1:p.Asn874Ser | |
| XM_006718958.1:c.2642A>G | XP_006719021.1:p.Asn881Ser | |
| XM_006718959.1:c.2642A>G | XP_006719022.1:p.Asn881Ser | |
| XM_006718960.1:c.2642A>G | XP_006719023.1:p.Asn881Ser | |
| XM_006718961.2:c.2621A>G | XP_006719024.1:p.Asn874Ser | |
| XM_006718962.1:c.2603A>G | XP_006719025.1:p.Asn868Ser | |
| NM_001273.4:c.2642A>G | NP_001264.2:p.Asn881Ser | |
| NM_001297553.2:c.2621A>G | NP_001284482.1:p.Asn874Ser | |
| NM_001363606.1:c.2603A>G | NP_001350535.1:p.Asn868Ser | |
| XM_017018725.1:c.2642A>G | XP_016874214.1:p.Asn881Ser | |
| XM_017018726.1:c.2642A>G | XP_016874215.1:p.Asn881Ser | |
| XM_017018727.1:c.2642A>G | XP_016874216.1:p.Asn881Ser | |
| XM_017018728.1:c.2642A>G | XP_016874217.1:p.Asn881Ser | |
| XM_017018729.1:c.2621A>G | XP_016874218.1:p.Asn874Ser | |
| XM_017018730.1:c.2603A>G | XP_016874219.1:p.Asn868Ser | |
| XM_017018731.1:c.2603A>G | XP_016874220.1:p.Asn868Ser | |
| XM_017018732.1:c.2582A>G | XP_016874221.1:p.Asn861Ser | |
| XM_017018733.1:c.2582A>G | XP_016874222.1:p.Asn861Ser | |
| XM_017018734.1:c.2582A>G | XP_016874223.1:p.Asn861Ser | |
| XM_024448802.1:c.2642A>G | XP_024304570.1:p.Asn881Ser | |
| XM_024448803.1:c.2621A>G | XP_024304571.1:p.Asn874Ser | |
| XM_024448804.1:c.2603A>G | XP_024304572.1:p.Asn868Ser | |
| XM_024448805.1:c.2582A>G | XP_024304573.1:p.Asn861Ser | |
| NM_001273.5:c.2642A>G MANE Select | NP_001264.2:p.Asn881Ser | |
| NM_001363606.2:c.2603A>G | NP_001350535.1:p.Asn868Ser |