HGVS | Genome Assembly |
---|---|
NC_000001.11:g.15440430G>A , CM000663.2:g.15440430G>A | GRCh38 |
NC_000001.10:g.15766926G>A , CM000663.1:g.15766926G>A | GRCh37 |
NC_000001.9:g.15639513G>A | NCBI36 |
NG_009253.1:g.6989G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375949.5:c.132+39G>A MANE Select | ENSP00000365116.4:n.132+39G>A | |
ENST00000375943.6:c.40+1926G>A | ENSP00000365110.2:n.40+1926G>A | |
ENST00000375949.4:c.132+39G>A | ENSP00000365116.4:n.132+39G>A | |
ENST00000476813.5:n.52+1926G>A | ||
ENST00000483406.1:n.42+39G>A | ||
NM_007272.2:c.132+39G>A | NP_009203.2:n.132+39G>A | |
XM_011540550.1:c.132+39G>A | XP_011538852.1:n.132+39G>A | |
NM_007272.3:c.132+39G>A MANE Select | NP_009203.2:n.132+39G>A |