HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15191659T>A , CM000681.2:g.15191659T>A | GRCh38 |
NC_000019.9:g.15302470T>A , CM000681.1:g.15302470T>A | GRCh37 |
NC_000019.8:g.15163470T>A | NCBI36 |
NG_009819.1:g.14323A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.803-2A>T MANE Select | ENSP00000263388.1:n.803-2A>T | |
ENST00000263388.6:c.803-2A>T | ENSP00000263388.1:n.803-2A>T | |
ENST00000601011.1:c.800-2A>T | ENSP00000473138.1:n.800-2A>T | |
NM_000435.2:c.803-2A>T | NP_000426.2:n.803-2A>T | |
XM_005259924.3:c.803-2A>T | XP_005259981.1:n.803-2A>T | |
XM_005259924.4:c.803-2A>T | XP_005259981.1:n.803-2A>T | |
NM_000435.3:c.803-2A>T MANE Select | NP_000426.2:n.803-2A>T |