Canonical Allele Identifier: CA360062220
Gene: HEXB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74685403T>A , CM000667.2:g.74685403T>A GRCh38
NC_000005.9:g.73981228T>A , CM000667.1:g.73981228T>A GRCh37
NC_000005.8:g.74016984T>A NCBI36
NG_009770.1:g.5260T>A
NG_009770.2:g.50381T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.143T>A MANE Select ENSP00000261416.7:p.Val48Asp
ENST00000261416.11:c.143T>A ENSP00000261416.7:p.Val48Asp
ENST00000511181.5:c.-376-3925T>A ENSP00000426285.1:n.-376-3925T>A
ENST00000513079.5:n.208T>A
ENST00000515528.1:n.198T>A
NM_000521.3:c.143T>A NP_000512.1:p.Val48Asp
NM_001292004.1:c.-376-3925T>A NP_001278933.1:n.-376-3925T>A
NM_000521.4:c.143T>A MANE Select NP_000512.2:p.Val48Asp
NM_001292004.2:c.-376-3925T>A NP_001278933.1:n.-376-3925T>A