Canonical Allele Identifier: CA560766121

Gene: HEXB

Linked Data

• dbSNP Id: rs930678778
• gnomAD v2: 5-73981405-C-A
• gnomAD v4: 5-74685580-C-A
• MyVariant Identifiers: chr5:g.73981405C>A (hg19) ; chr5:g.74685580C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74685580C>A , CM000667.2:g.74685580C>A	GRCh38
NC_000005.9:g.73981405C>A , CM000667.1:g.73981405C>A	GRCh37
NC_000005.8:g.74017161C>A	NCBI36
NG_009770.1:g.5437C>A
NG_009770.2:g.50558C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261416.12:c.299+21C>A MANE Select	ENSP00000261416.7:n.299+21C>A
ENST00000261416.11:c.299+21C>A	ENSP00000261416.7:n.299+21C>A
ENST00000511181.5:c.-376-3748C>A	ENSP00000426285.1:n.-376-3748C>A
ENST00000513079.5:n.364+21C>A
ENST00000515528.1:n.354+21C>A
NM_000521.3:c.299+21C>A	NP_000512.1:n.299+21C>A
NM_001292004.1:c.-376-3748C>A	NP_001278933.1:n.-376-3748C>A
NM_000521.4:c.299+21C>A MANE Select	NP_000512.2:n.299+21C>A
NM_001292004.2:c.-376-3748C>A	NP_001278933.1:n.-376-3748C>A