HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652669A>T , CM000663.2:g.171652669A>T | GRCh38 |
NC_000001.10:g.171621809A>T , CM000663.1:g.171621809A>T | GRCh37 |
NC_000001.9:g.169888432A>T | NCBI36 |
NG_008859.1:g.4965T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-58T>A MANE Select | ENSP00000037502.5:n.-58T>A | |
ENST00000037502.10:c.-58T>A | ENSP00000037502.5:n.-58T>A | |
NM_000261.2:c.-58T>A MANE Select | NP_000252.1:n.-58T>A |