HGVS | Genome Assembly |
---|---|
NC_000009.12:g.130862907T>A , CM000671.2:g.130862907T>A | GRCh38 |
NC_000009.11:g.133738294T>A , CM000671.1:g.133738294T>A | GRCh37 |
NC_000009.10:g.132728115T>A | NCBI36 |
NG_012034.1:g.154027T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372348.9:c.751T>A | ENSP00000361423.2:p.Tyr251Asn | |
ENST00000318560.6:c.694T>A MANE Select | ENSP00000323315.5:p.Tyr232Asn | |
ENST00000372348.7:c.751T>A | ENSP00000361423.2:p.Tyr251Asn | |
ENST00000318560.5:c.694T>A | ENSP00000323315.5:p.Tyr232Asn | |
ENST00000372348.6:c.751T>A | ENSP00000361423.2:p.Tyr251Asn | |
NM_005157.5:c.694T>A | NP_005148.2:p.Tyr232Asn | |
NM_007313.2:c.751T>A | NP_009297.2:p.Tyr251Asn | |
NM_005157.6:c.694T>A MANE Select | NP_005148.2:p.Tyr232Asn | |
NM_007313.3:c.751T>A | NP_009297.2:p.Tyr251Asn |