Linked Data
dbSNP Id:
rs896130699
gnomAD v2:
6-31691816-G-C
gnomAD v3:
6-31724039-G-C
gnomAD v4:
6-31724039-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31724039G>C , CM000668.2:g.31724039G>C | GRCh38 |
| NC_000006.11:g.31691816G>C , CM000668.1:g.31691816G>C | GRCh37 |
| NC_000006.10:g.31799795G>C | NCBI36 |
| NG_029044.1:g.5696G>C | |
| NG_029044.2:g.5696G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649779.1:c.409+53G>C MANE Select | ENSP00000497720.1:n.409+53G>C | |
| ENST00000375804.6:c.409+53G>C | ENSP00000364962.2:n.409+53G>C | |
| ENST00000375805.6:c.409+53G>C | ENSP00000364963.2:n.409+53G>C | |
| ENST00000375806.2:c.409+53G>C | ENSP00000364964.2:n.409+53G>C | |
| ENST00000375809.7:c.409+53G>C | ENSP00000364967.3:n.409+53G>C | |
| ENST00000375810.8:c.409+53G>C | ENSP00000364968.4:n.409+53G>C | |
| ENST00000375814.7:c.409+53G>C | ENSP00000364972.3:n.409+53G>C | |
| ENST00000460663.5:n.616+53G>C | ||
| ENST00000466312.5:n.413+53G>C | ||
| ENST00000471545.1:n.409+53G>C | ||
| ENST00000480039.5:c.409+53G>C | ENSP00000419306.1:n.409+53G>C | |
| ENST00000485548.5:c.269-120G>C | ENSP00000420355.1:n.269-120G>C | |
| NM_025260.3:c.409+53G>C | NP_079536.2:n.409+53G>C | |
| NM_138272.2:c.409+53G>C | NP_612116.1:n.409+53G>C | |
| NM_138273.2:c.409+53G>C | NP_612117.1:n.409+53G>C | |
| NM_138274.2:c.409+53G>C | NP_612118.1:n.409+53G>C | |
| NM_138275.2:c.409+53G>C | NP_612119.1:n.409+53G>C | |
| NM_138277.2:c.409+53G>C | NP_612121.1:n.409+53G>C | |
| XM_011514920.1:c.457+53G>C | XP_011513222.1:n.457+53G>C | |
| XM_011514921.1:c.457+53G>C | XP_011513223.1:n.457+53G>C | |
| XM_011514920.2:c.457+53G>C | XP_011513222.1:n.457+53G>C | |
| XM_011514921.2:c.457+53G>C | XP_011513223.1:n.457+53G>C | |
| XM_017011330.1:c.457+53G>C | XP_016866819.1:n.457+53G>C | |
| XM_017011331.1:c.409+53G>C | XP_016866820.1:n.409+53G>C | |
| XM_017011332.1:c.457+53G>C | XP_016866821.1:n.457+53G>C | |
| XM_017011333.1:c.457+53G>C | XP_016866822.1:n.457+53G>C | |
| NM_025260.4:c.409+53G>C | NP_079536.2:n.409+53G>C | |
| NM_138272.3:c.409+53G>C MANE Select | NP_612116.1:n.409+53G>C | |
| NM_138273.3:c.409+53G>C | NP_612117.1:n.409+53G>C | |
| NM_138274.3:c.409+53G>C | NP_612118.1:n.409+53G>C | |
| NM_138275.3:c.409+53G>C | NP_612119.1:n.409+53G>C | |
| NM_138277.3:c.409+53G>C | NP_612121.1:n.409+53G>C |