Linked Data
dbSNP Id:
rs978593507
gnomAD v2:
4-111542274-A-T
gnomAD v3:
4-110621118-A-T
gnomAD v4:
4-110621118-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.110621118A>T , CM000666.2:g.110621118A>T | GRCh38 |
| NC_000004.11:g.111542274A>T , CM000666.1:g.111542274A>T | GRCh37 |
| NC_000004.10:g.111761723A>T | NCBI36 |
| NG_007120.1:g.21235T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000613094.5:c.185-2430T>A | ENSP00000484763.2:n.185-2430T>A | |
| ENST00000614423.5:c.309+46T>A | ENSP00000481951.2:n.309+46T>A | |
| ENST00000616641.5:n.377+46T>A | ||
| ENST00000644488.2:n.381+46T>A | ||
| ENST00000394595.8:c.390+46T>A | ENSP00000378095.4:n.390+46T>A | |
| ENST00000644488.1:n.453+46T>A | ||
| ENST00000644743.1:c.411+46T>A MANE Select | ENSP00000495061.1:n.411+46T>A | |
| ENST00000645131.1:n.342+46T>A | ||
| ENST00000306732.7:c.411+46T>A | ENSP00000304169.3:n.411+46T>A | |
| ENST00000354925.6:c.390+46T>A | ENSP00000347004.2:n.390+46T>A | |
| ENST00000355080.9:c.252+46T>A | ENSP00000347192.5:n.252+46T>A | |
| ENST00000394595.7:c.185-2430T>A | ENSP00000378095.3:n.185-2430T>A | |
| ENST00000394598.6:c.390+46T>A | ENSP00000378097.2:n.390+46T>A | |
| ENST00000511837.5:c.390+46T>A | ENSP00000421454.1:n.390+46T>A | |
| ENST00000511990.1:c.252+46T>A | ENSP00000424142.1:n.252+46T>A | |
| ENST00000557119.2:c.457T>A | ENSP00000475617.1:p.Trp153Arg | |
| ENST00000613094.4:c.390+46T>A | ENSP00000484763.1:n.390+46T>A | |
| ENST00000614423.4:c.390+46T>A | ENSP00000481951.1:n.390+46T>A | |
| ENST00000616641.4:c.252+46T>A | ENSP00000484909.1:n.252+46T>A | |
| NM_000325.5:c.411+46T>A | NP_000316.2:n.411+46T>A | |
| NM_001204397.1:c.390+46T>A | NP_001191326.1:n.390+46T>A | |
| NM_001204398.1:c.390+46T>A | NP_001191327.1:n.390+46T>A | |
| NM_001204399.1:c.252+46T>A | NP_001191328.1:n.252+46T>A | |
| NM_153426.2:c.390+46T>A | NP_700475.1:n.390+46T>A | |
| NM_153427.2:c.252+46T>A | NP_700476.1:n.252+46T>A | |
| XM_006714235.2:c.390+46T>A | XP_006714298.1:n.390+46T>A | |
| XM_011532027.1:c.252+46T>A | XP_011530329.1:n.252+46T>A | |
| XM_024454090.1:c.57+46T>A | XP_024309858.1:n.57+46T>A | |
| NM_000325.6:c.411+46T>A MANE Select | NP_000316.2:n.411+46T>A | |
| NM_001204397.2:c.390+46T>A | NP_001191326.1:n.390+46T>A | |
| NM_153426.3:c.390+46T>A | NP_700475.1:n.390+46T>A | |
| NM_153427.3:c.252+46T>A | NP_700476.1:n.252+46T>A |