HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55157625C= , CM000681.2:g.55157625C= | GRCh38 |
NC_000019.9:g.55668993C= , CM000681.1:g.55668993C= | GRCh37 |
NC_000019.8:g.60360805C= | NCBI36 |
NG_007866.2:g.5108G= , LRG_432:g.5108G= | |
NG_032759.1:g.14098G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.-36G= MANE Select | ENSP00000341838.5:n.-36G= | |
ENST00000665070.1:c.-36G= | ENSP00000499482.1:n.-36G= | |
ENST00000344887.9:c.-36G= | ENSP00000341838.5:n.-36G= | |
ENST00000586446.1:n.108G= | ||
ENST00000587176.5:n.149G= | ||
ENST00000587871.1:c.585G= | ||
ENST00000590463.1:n.92G= | ||
NM_000363.4:c.-36G= , LRG_432t1:c.-36G= | NP_000354.4:n.-36G= | |
NM_000363.5:c.-36G= MANE Select | NP_000354.4:n.-36G= |