HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188989428A>T , CM000664.2:g.188989428A>T | GRCh38 |
NC_000002.11:g.189854154A>T , CM000664.1:g.189854154A>T | GRCh37 |
NC_000002.10:g.189562399A>T | NCBI36 |
NG_007404.1:g.20056A>T , LRG_3:g.20056A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.669A>T | ENSP00000415346.2:p.Pro223= | |
ENST00000304636.9:c.669A>T MANE Select | ENSP00000304408.4:p.Pro223= | |
ENST00000304636.7:c.669A>T | ENSP00000304408.3:p.Pro223= | |
ENST00000317840.9:c.669A>T | ENSP00000315243.6:p.Pro223= | |
NM_000090.3:c.669A>T , LRG_3t1:c.669A>T | NP_000081.1:p.Pro223= | |
NM_000090.4:c.669A>T MANE Select | NP_000081.2:p.Pro223= |