Linked Data
dbSNP Id:
rs4857037
gnomAD v2:
3-93627812-G-A
gnomAD v3:
3-93908968-G-A
gnomAD v4:
3-93908968-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.93908968G>A , CM000665.2:g.93908968G>A | GRCh38 |
| NC_000003.11:g.93627812G>A , CM000665.1:g.93627812G>A | GRCh37 |
| NC_000003.10:g.95110502G>A | NCBI36 |
| NG_009813.1:g.70123C>T , LRG_572:g.70123C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000348974.5:c.346+1651C>T | ENSP00000330021.7:n.346+1651C>T | |
| ENST00000394236.9:c.346+1651C>T MANE Select | ENSP00000377783.3:n.346+1651C>T | |
| ENST00000407433.6:c.346+1651C>T | ENSP00000385794.2:n.346+1651C>T | |
| ENST00000472684.2:c.-48+1651C>T | ENSP00000419616.2:n.-48+1651C>T | |
| ENST00000647936.1:c.346+1651C>T | ENSP00000496822.1:n.346+1651C>T | |
| ENST00000648381.1:n.514+1651C>T | ||
| ENST00000648853.1:c.304+1651C>T | ENSP00000497262.1:n.304+1651C>T | |
| ENST00000649103.1:c.445+1651C>T | ENSP00000497962.1:n.445+1651C>T | |
| ENST00000650591.1:c.442+1651C>T | ENSP00000497376.1:n.442+1651C>T | |
| ENST00000348974.4:c.442+1651C>T | ENSP00000330021.6:n.442+1651C>T | |
| ENST00000394236.7:c.346+1651C>T | ENSP00000377783.3:n.346+1651C>T | |
| ENST00000407433.5:c.-48+1651C>T | ENSP00000385794.1:n.-48+1651C>T | |
| ENST00000472684.1:c.-48+1651C>T | ENSP00000419616.1:n.-48+1651C>T | |
| ENST00000488658.1:n.539+1651C>T | ||
| NM_000313.3:c.346+1651C>T , LRG_572t1:c.346+1651C>T | NP_000304.2:n.346+1651C>T | |
| NM_001314077.1:c.442+1651C>T , LRG_572t2:c.442+1651C>T | NP_001301006.1:n.442+1651C>T | |
| NM_000313.4:c.346+1651C>T MANE Select | NP_000304.2:n.346+1651C>T | |
| NM_001314077.2:c.442+1651C>T | NP_001301006.1:n.442+1651C>T |