HGVS | Genome Assembly |
---|---|
NC_000009.12:g.129814190T>A , CM000671.2:g.129814190T>A | GRCh38 |
NC_000009.11:g.132576469T>A , CM000671.1:g.132576469T>A | GRCh37 |
NC_000009.10:g.131616290T>A | NCBI36 |
NG_008049.1:g.14973A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000351698.5:c.781A>T MANE Select | ENSP00000345719.4:p.Asn261Tyr | |
ENST00000651202.1:c.*49A>T | ENSP00000498222.1:n.*49A>T | |
ENST00000351698.4:c.781A>T | ENSP00000345719.4:p.Asn261Tyr | |
ENST00000474192.1:n.365A>T | ||
NM_000113.2:c.781A>T | NP_000104.1:p.Asn261Tyr | |
XR_929731.1:n.1108A>T | ||
XR_929731.3:n.976A>T | ||
NM_000113.3:c.781A>T MANE Select | NP_000104.1:p.Asn261Tyr |