HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128345177G>T , CM000671.2:g.128345177G>T | GRCh38 |
NC_000009.11:g.131107456G>T , CM000671.1:g.131107456G>T | GRCh37 |
NC_000009.10:g.130147277G>T | NCBI36 |
NG_017057.1:g.9618G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000300456.5:c.184G>T MANE Select | ENSP00000300456.3:p.Val62Leu | |
ENST00000300456.4:c.184G>T | ENSP00000300456.3:p.Val62Leu | |
ENST00000372870.5:c.231+1896G>T | ENSP00000361961.1:n.231+1896G>T | |
NM_005094.3:c.184G>T | NP_005085.2:p.Val62Leu | |
XM_017014222.1:c.184G>T | XP_016869711.1:p.Val62Leu | |
XM_024447391.1:c.184G>T | XP_024303159.1:p.Val62Leu | |
NM_005094.4:c.184G>T MANE Select | NP_005085.2:p.Val62Leu |