HGVS | Genome Assembly |
---|---|
NC_000013.11:g.92670899T>C , CM000675.2:g.92670899T>C | GRCh38 |
NC_000013.10:g.93323152T>C , CM000675.1:g.93323152T>C | GRCh37 |
NC_000013.9:g.92121153T>C | NCBI36 |
NG_009370.1:g.1277218T>C | |
NG_009370.2:g.1277219T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377067.9:c.1562-195383T>C MANE Select | ENSP00000366267.3:n.1562-195383T>C | |
ENST00000377067.8:c.1562-195383T>C | ENSP00000366267.3:n.1562-195383T>C | |
NM_004466.5:c.1562-195383T>C | NP_004457.1:n.1562-195383T>C | |
XR_931643.1:n.173+6619A>G | ||
XR_931644.1:n.173+6619A>G | ||
XM_017020435.2:c.1562-79065T>C | XP_016875924.1:n.1562-79065T>C | |
XR_931643.3:n.2210+6619A>G | ||
XR_931644.2:n.2210+6619A>G | ||
NM_004466.6:c.1562-195383T>C MANE Select | NP_004457.1:n.1562-195383T>C |