HGVS | Genome Assembly |
---|---|
NC_000020.11:g.61531848C= , CM000682.2:g.61531848C= | GRCh38 |
NC_000020.10:g.60106904C= , CM000682.1:g.60106904C= | GRCh37 |
NC_000020.9:g.59540299C= | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614565.5:c.170-211715C= MANE Select | ENSP00000484928.1:n.170-211715C= | |
ENST00000614565.4:c.170-211715C= | ENSP00000484928.1:n.170-211715C= | |
NM_001252338.2:c.58+32356C= | NP_001239267.1:n.58+32356C= | |
NM_001794.4:c.170-211715C= | NP_001785.2:n.170-211715C= | |
NM_001794.5:c.170-211715C= MANE Select | NP_001785.2:n.170-211715C= |