HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87727596T>A , CM000672.2:g.87727596T>A | GRCh38 |
NC_000010.10:g.89487353T>A , CM000672.1:g.89487353T>A | GRCh37 |
NC_000010.9:g.89477333T>A | NCBI36 |
NG_012150.1:g.72878T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.1086+107T>A MANE Select | ENSP00000406157.1:n.1086+107T>A | |
ENST00000361175.8:c.1071+107T>A | ENSP00000354436.4:n.1071+107T>A | |
ENST00000456849.1:c.1086+107T>A | ENSP00000406157.1:n.1086+107T>A | |
NM_001015880.1:c.1086+107T>A | NP_001015880.1:n.1086+107T>A | |
NM_004670.3:c.1071+107T>A | NP_004661.2:n.1071+107T>A | |
NM_001015880.2:c.1086+107T>A MANE Select | NP_001015880.1:n.1086+107T>A | |
NM_004670.4:c.1071+107T>A | NP_004661.2:n.1071+107T>A |