Canonical Allele Identifier: CA444849964
Gene: HEXB HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.73981235C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74685410C>G , CM000667.2:g.74685410C>G GRCh38
NC_000005.9:g.73981235C>G , CM000667.1:g.73981235C>G GRCh37
NC_000005.8:g.74016991C>G NCBI36
NG_009770.1:g.5267C>G
NG_009770.2:g.50388C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.150C>G MANE Select ENSP00000261416.7:p.Ala50=
ENST00000261416.11:c.150C>G ENSP00000261416.7:p.Ala50=
ENST00000511181.5:c.-376-3918C>G ENSP00000426285.1:n.-376-3918C>G
ENST00000513079.5:n.215C>G
ENST00000515528.1:n.205C>G
NM_000521.3:c.150C>G NP_000512.1:p.Ala50=
NM_001292004.1:c.-376-3918C>G NP_001278933.1:n.-376-3918C>G
NM_000521.4:c.150C>G MANE Select NP_000512.2:p.Ala50=
NM_001292004.2:c.-376-3918C>G NP_001278933.1:n.-376-3918C>G
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