HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101686817A>T , CM000671.2:g.101686817A>T | GRCh38 |
NC_000009.11:g.104449099A>T , CM000671.1:g.104449099A>T | GRCh37 |
NC_000009.10:g.103488920A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.1083T>A MANE Select | ENSP00000355155.3:p.Asn361Lys | |
ENST00000361820.3:c.1083T>A | ENSP00000355155.3:p.Asn361Lys | |
NM_133445.2:c.1083T>A | NP_597702.2:p.Asn361Lys | |
XM_011518211.1:c.1083T>A | XP_011516513.1:p.Asn361Lys | |
XM_011518212.1:c.1083T>A | XP_011516514.1:p.Asn361Lys | |
XR_929711.1:n.1170T>A | ||
XM_011518211.2:c.1083T>A | XP_011516513.1:p.Asn361Lys | |
NM_133445.3:c.1083T>A MANE Select | NP_597702.2:p.Asn361Lys |