HGVS | Genome Assembly |
---|---|
NC_000001.11:g.56500742C>A , CM000663.2:g.56500742C>A | GRCh38 |
NC_000001.10:g.56966414C>A , CM000663.1:g.56966414C>A | GRCh37 |
NC_000001.9:g.56739002C>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371250.4:c.811-4066G>T MANE Select | ENSP00000360296.3:n.811-4066G>T | |
ENST00000641109.1:c.220-4066G>T | ENSP00000493138.1:n.220-4066G>T | |
ENST00000641494.1:c.65-4066G>T | ||
ENST00000642129.1:c.455-4066G>T | ||
ENST00000371250.3:c.811-4066G>T | ENSP00000360296.3:n.811-4066G>T | |
ENST00000459962.1:n.1797-4066G>T | ||
ENST00000472957.1:n.296-4066G>T | ||
NM_003713.4:c.811-4066G>T | NP_003704.3:n.811-4066G>T | |
NM_003713.5:c.811-4066G>T MANE Select | NP_003704.3:n.811-4066G>T |