HGVS | Genome Assembly |
---|---|
NC_000001.11:g.206776084T>A , CM000663.2:g.206776084T>A | GRCh38 |
NC_000001.10:g.206949429T>A , CM000663.1:g.206949429T>A | GRCh37 |
NC_000001.9:g.205016052T>A | NCBI36 |
NG_012088.1:g.1411A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000659997.3:c.-149+5006T>A MANE Select | ENSP00000499459.2:n.-149+5006T>A | |
ENST00000656872.2:c.-149+5254T>A | ENSP00000499487.2:n.-149+5254T>A | |
ENST00000659997.2:c.-149+5006T>A | ENSP00000499459.2:n.-149+5006T>A | |
ENST00000662320.1:n.67+5254T>A | ||
NM_153758.3:c.-35+5006T>A | NP_715639.1:n.-35+5006T>A | |
NM_001393490.1:c.-149+5254T>A | NP_001380419.1:n.-149+5254T>A | |
NM_153758.5:c.-149+5006T>A MANE Select | NP_715639.2:n.-149+5006T>A |