HGVS | Genome Assembly |
---|---|
NC_000008.11:g.54626345T= , CM000670.2:g.54626345T= | GRCh38 |
NC_000008.10:g.55538905T= , CM000670.1:g.55538905T= | GRCh37 |
NC_000008.9:g.55701458T= | NCBI36 |
NG_009840.1:g.15279T= | |
NG_009840.2:g.15279T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000220676.2:c.2463T= MANE Select | ENSP00000220676.1:p.His821= | |
ENST00000636932.1:c.787+4057T= | ENSP00000489857.1:n.787+4057T= | |
ENST00000637698.1:c.787+4057T= | ENSP00000490104.1:n.787+4057T= | |
ENST00000220676.1:c.2463T= | ENSP00000220676.1:p.His821= | |
NM_006269.1:c.2463T= | NP_006260.1:p.His821= | |
XM_017013721.1:c.2484T= | XP_016869210.1:p.His828= | |
XM_017013722.1:c.2463T= | XP_016869211.1:p.His821= | |
NM_001375654.1:c.787+4057T= | NP_001362583.1:n.787+4057T= | |
NM_006269.2:c.2463T= MANE Select | NP_006260.1:p.His821= |