HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23421027A= , CM000676.2:g.23421027A= | GRCh38 |
NC_000014.8:g.23890236A= , CM000676.1:g.23890236A= | GRCh37 |
NC_000014.7:g.22960076A= | NCBI36 |
NG_007884.1:g.19635T= , LRG_384:g.19635T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.3267T= MANE Select | ENSP00000347507.3:p.Ala1089= | |
ENST00000355349.3:c.3267T= | ENSP00000347507.3:p.Ala1089= | |
NM_000257.3:c.3267T= | NP_000248.2:p.Ala1089= | |
XR_245686.3:n.3375T= | ||
XM_017021340.1:c.3267T= | XP_016876829.1:p.Ala1089= | |
NM_000257.4:c.3267T= MANE Select | NP_000248.2:p.Ala1089= |