HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196996046T= , CM000663.2:g.196996046T= | GRCh38 |
NC_000001.10:g.196965176T= , CM000663.1:g.196965176T= | GRCh37 |
NC_000001.9:g.195231799T= | NCBI36 |
NG_016365.1:g.23510T= , LRG_227:g.23510T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.560T= | ENSP00000514393.1:p.Ile187= | |
ENST00000699467.1:n.884T= | ||
ENST00000699468.1:c.-24-68T= | ENSP00000514394.1:n.-24-68T= | |
ENST00000256785.5:c.815T= MANE Select | ENSP00000256785.4:p.Ile272= | |
ENST00000256785.4:c.815T= | ENSP00000256785.4:p.Ile272= | |
NM_030787.3:c.815T= , LRG_227t1:c.815T= | NP_110414.1:p.Ile272= | |
XM_011510020.1:c.824T= | XP_011508322.1:p.Ile275= | |
XM_011510020.2:c.824T= | XP_011508322.1:p.Ile275= | |
NM_030787.4:c.815T= MANE Select | NP_110414.1:p.Ile272= |