Linked Data
ClinVar Variation Id:
6867
dbSNP Id:
rs137853042
ExAC:
19:36322260 G / A
gnomAD v2:
19-36322260-G-A
gnomAD v3:
19-35831358-G-A
gnomAD v4:
19-35831358-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35831358G>A , CM000681.2:g.35831358G>A | GRCh38 |
| NC_000019.9:g.36322260G>A , CM000681.1:g.36322260G>A | GRCh37 |
| NC_000019.8:g.41014100G>A | NCBI36 |
| NG_013356.2:g.42930C>T , LRG_693:g.42930C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000378910.10:c.3325C>T MANE Select | ENSP00000368190.4:p.Arg1109Ter | |
| ENST00000353632.6:c.3205C>T | ENSP00000343634.5:p.Arg1069Ter | |
| ENST00000378910.9:c.3325C>T | ENSP00000368190.4:p.Arg1109Ter | |
| NM_004646.3:c.3325C>T , LRG_693t1:c.3325C>T | NP_004637.1:p.Arg1109Ter | |
| NM_004646.4:c.3325C>T MANE Select | NP_004637.1:p.Arg1109Ter |