Linked Data
dbSNP Id:
rs2068754568
gnomAD v3:
19-53900419-G-T
gnomAD v4:
19-53900419-G-T
MyVariant Identifiers:
chr19:g.54403673G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.53900419G>T , CM000681.2:g.53900419G>T | GRCh38 |
| NC_000019.9:g.54403673G>T , CM000681.1:g.54403673G>T | GRCh37 |
| NC_000019.8:g.59095485G>T | NCBI36 |
| NG_009114.1:g.23207G>T , LRG_669:g.23207G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682028.1:c.1374G>T | ENSP00000507230.1:p.Ala458= | |
| ENST00000682268.1:n.1672G>T | ||
| ENST00000682676.1:n.775G>T | ||
| ENST00000682902.1:n.1676G>T | ||
| ENST00000683513.1:c.1374G>T | ENSP00000506809.1:p.Ala458= | |
| ENST00000263431.4:c.1374G>T MANE Select | ENSP00000263431.3:p.Ala458= | |
| ENST00000263431.3:c.1374G>T | ENSP00000263431.3:p.Ala458= | |
| NM_001316329.1:c.1374G>T | NP_001303258.1:p.Ala458= | |
| NM_002739.3:c.1374G>T , LRG_669t1:c.1374G>T | NP_002730.1:p.Ala458= | |
| NM_002739.4:c.1374G>T | NP_002730.1:p.Ala458= | |
| XM_011527108.1:c.465G>T | XP_011525410.1:p.Ala155= | |
| NM_002739.5:c.1374G>T MANE Select | NP_002730.1:p.Ala458= | |
| NM_001316329.2:c.1374G>T | NP_001303258.1:p.Ala458= |