Canonical Allele Identifier: CA360070178
Gene: HEXB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74718807G>T , CM000667.2:g.74718807G>T GRCh38
NC_000005.9:g.74014632G>T , CM000667.1:g.74014632G>T GRCh37
NC_000005.8:g.74050388G>T NCBI36
NG_009770.1:g.38664G>T
NG_009770.2:g.83785G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261416.12:c.1253G>T MANE Select ENSP00000261416.7:p.Gly418Val
ENST00000261416.11:c.1253G>T ENSP00000261416.7:p.Gly418Val
ENST00000503312.5:c.129G>T
ENST00000504459.5:n.450G>T
ENST00000511181.5:c.578G>T ENSP00000426285.1:p.Gly193Val
ENST00000513336.5:c.189G>T
ENST00000513539.1:n.74-102G>T
NM_000521.3:c.1253G>T NP_000512.1:p.Gly418Val
NM_001292004.1:c.578G>T NP_001278933.1:p.Gly193Val
NM_000521.4:c.1253G>T MANE Select NP_000512.2:p.Gly418Val
NM_001292004.2:c.578G>T NP_001278933.1:p.Gly193Val