HGVS | Genome Assembly |
---|---|
NC_000009.12:g.101615912A>T , CM000671.2:g.101615912A>T | GRCh38 |
NC_000009.11:g.104378194A>T , CM000671.1:g.104378194A>T | GRCh37 |
NC_000009.10:g.103418015A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361820.6:c.2615-2385T>A MANE Select | ENSP00000355155.3:n.2615-2385T>A | |
ENST00000361820.3:c.2615-2385T>A | ENSP00000355155.3:n.2615-2385T>A | |
NM_133445.2:c.2615-2385T>A | NP_597702.2:n.2615-2385T>A | |
XM_011518211.1:c.2615-2385T>A | XP_011516513.1:n.2615-2385T>A | |
XM_011518212.1:c.2615-2385T>A | XP_011516514.1:n.2615-2385T>A | |
XR_929711.1:n.2702-2385T>A | ||
XM_011518211.2:c.2615-2385T>A | XP_011516513.1:n.2615-2385T>A | |
NM_133445.3:c.2615-2385T>A MANE Select | NP_597702.2:n.2615-2385T>A |