HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152310973C>T , CM000663.2:g.152310973C>T | GRCh38 |
NC_000001.10:g.152283449C>T , CM000663.1:g.152283449C>T | GRCh37 |
NC_000001.9:g.150550073C>T | NCBI36 |
NG_016190.1:g.19231G>A , LRG_1028:g.19231G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.3913G>A MANE Select | ENSP00000357789.1:p.Gly1305Ser | |
ENST00000368799.1:c.3913G>A | ENSP00000357789.1:p.Gly1305Ser | |
NM_002016.1:c.3913G>A , LRG_1028t1:c.3913G>A | NP_002007.1:p.Gly1305Ser | |
XM_011509329.1:c.3913G>A | XP_011507631.1:p.Gly1305Ser | |
NM_002016.2:c.3913G>A MANE Select | NP_002007.1:p.Gly1305Ser |