Linked Data
dbSNP Id:
rs570814409
gnomAD v2:
12-80752668-A-G
gnomAD v3:
12-80358888-A-G
gnomAD v4:
12-80358888-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.80358888A>G , CM000674.2:g.80358888A>G | GRCh38 |
| NC_000012.11:g.80752668A>G , CM000674.1:g.80752668A>G | GRCh37 |
| NC_000012.10:g.79276799A>G | NCBI36 |
| NG_033008.1:g.154436A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547103.7:c.6255A>G MANE Select | ENSP00000447211.2:p.Pro2085= | |
| ENST00000642294.1:c.195A>G | ENSP00000493572.1:p.Pro65= | |
| ENST00000646859.1:c.6120A>G | ENSP00000496036.1:p.Pro2040= | |
| ENST00000298820.7:c.1527+113A>G | ||
| ENST00000458043.6:c.6228A>G | ENSP00000400895.2:p.Pro2076= | |
| ENST00000546620.5:n.511A>G | ||
| ENST00000547103.5:c.6192A>G | ENSP00000447211.1:p.Pro2064= | |
| ENST00000550182.2:c.279A>G | ENSP00000449641.1:p.Pro93= | |
| ENST00000551340.5:c.383A>G | ||
| NM_173591.3:c.6228A>G | NP_775862.3:p.Pro2076= | |
| XM_005268802.2:c.6279A>G | XP_005268859.1:p.Pro2093= | |
| XM_011538191.1:c.6279A>G | XP_011536493.1:p.Pro2093= | |
| XM_011538192.1:c.6126A>G | XP_011536494.1:p.Pro2042= | |
| XM_011538193.1:c.5913A>G | XP_011536495.1:p.Pro1971= | |
| XM_005268802.3:c.6279A>G | XP_005268859.1:p.Pro2093= | |
| XM_011538192.2:c.6126A>G | XP_011536494.1:p.Pro2042= | |
| NM_001368062.1:c.6093A>G | NP_001354991.1:p.Pro2031= | |
| NM_001368062.3:c.6120A>G | NP_001354991.2:p.Pro2040= | |
| NM_001378609.3:c.6255A>G MANE Select | NP_001365538.2:p.Pro2085= | |
| NM_001378610.3:c.6255A>G | NP_001365539.2:p.Pro2085= | |
| NM_173591.7:c.6255A>G | NP_775862.4:p.Pro2085= |