HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20759982A= , CM000686.2:g.20759982A= | GRCh38 |
NC_000024.9:g.22921868A= , CM000686.1:g.22921868A= | GRCh37 |
NC_000024.8:g.21331256A= | NCBI36 |
NG_032924.1:g.8915A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000629237.2:c.196A= MANE Select | ENSP00000486252.1:p.Met66= | |
ENST00000629237.1:c.196A= | ENSP00000486252.1:p.Met66= | |
NM_001039567.2:c.196A= | NP_001034656.1:p.Met66= | |
XM_011531423.1:c.145A= | XP_011529725.1:p.Met49= | |
NM_001039567.3:c.196A= MANE Select | NP_001034656.1:p.Met66= |