Canonical Allele Identifier: CA360070184
Gene: HEXB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74718810C>T , CM000667.2:g.74718810C>T GRCh38
NC_000005.9:g.74014635C>T , CM000667.1:g.74014635C>T GRCh37
NC_000005.8:g.74050391C>T NCBI36
NG_009770.1:g.38667C>T
NG_009770.2:g.83788C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261416.12:c.1256C>T MANE Select ENSP00000261416.7:p.Thr419Ile
ENST00000261416.11:c.1256C>T ENSP00000261416.7:p.Thr419Ile
ENST00000503312.5:c.132C>T
ENST00000504459.5:n.453C>T
ENST00000511181.5:c.581C>T ENSP00000426285.1:p.Thr194Ile
ENST00000513336.5:c.192C>T
ENST00000513539.1:n.74-99C>T
NM_000521.3:c.1256C>T NP_000512.1:p.Thr419Ile
NM_001292004.1:c.581C>T NP_001278933.1:p.Thr194Ile
NM_000521.4:c.1256C>T MANE Select NP_000512.2:p.Thr419Ile
NM_001292004.2:c.581C>T NP_001278933.1:p.Thr194Ile