HGVS | Genome Assembly |
---|---|
NC_000013.11:g.92670915C= , CM000675.2:g.92670915C= | GRCh38 |
NC_000013.10:g.93323168C= , CM000675.1:g.93323168C= | GRCh37 |
NC_000013.9:g.92121169C= | NCBI36 |
NG_009370.1:g.1277234C= | |
NG_009370.2:g.1277235C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377067.9:c.1562-195367C= MANE Select | ENSP00000366267.3:n.1562-195367C= | |
ENST00000377067.8:c.1562-195367C= | ENSP00000366267.3:n.1562-195367C= | |
NM_004466.5:c.1562-195367C= | NP_004457.1:n.1562-195367C= | |
XR_931643.1:n.173+6603G= | ||
XR_931644.1:n.173+6603G= | ||
XM_017020435.2:c.1562-79049C= | XP_016875924.1:n.1562-79049C= | |
XR_931643.3:n.2210+6603G= | ||
XR_931644.2:n.2210+6603G= | ||
NM_004466.6:c.1562-195367C= MANE Select | NP_004457.1:n.1562-195367C= |