HGVS | Genome Assembly |
---|---|
NC_000012.12:g.128701853T>A , CM000674.2:g.128701853T>A | GRCh38 |
NC_000012.11:g.129186398T>A , CM000674.1:g.129186398T>A | GRCh37 |
NC_000012.10:g.127752351T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435159.3:c.2122-3237T>A MANE Select | ENSP00000410852.2:n.2122-3237T>A | |
ENST00000435159.2:c.2122-3237T>A | ENSP00000410852.2:n.2122-3237T>A | |
NM_001136103.2:c.2122-3237T>A | NP_001129575.2:n.2122-3237T>A | |
XM_011538998.1:c.2062-3237T>A | XP_011537300.1:n.2062-3237T>A | |
XM_011538998.2:c.2062-3237T>A | XP_011537300.1:n.2062-3237T>A | |
XR_001748922.1:n.2355-2799T>A | ||
NM_001136103.3:c.2122-3237T>A MANE Select | NP_001129575.2:n.2122-3237T>A | |
NM_001387058.1:c.2062-3237T>A | NP_001373987.1:n.2062-3237T>A |