Canonical Allele Identifier: CA360062570

Gene: HEXB

Linked Data

• dbSNP Id: rs1580377479
• MyVariant Identifiers: chr5:g.73981386T>G (hg19) ; chr5:g.74685561T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74685561T>G , CM000667.2:g.74685561T>G	GRCh38
NC_000005.9:g.73981386T>G , CM000667.1:g.73981386T>G	GRCh37
NC_000005.8:g.74017142T>G	NCBI36
NG_009770.1:g.5418T>G
NG_009770.2:g.50539T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261416.12:c.299+2T>G MANE Select	ENSP00000261416.7:n.299+2T>G
ENST00000261416.11:c.299+2T>G	ENSP00000261416.7:n.299+2T>G
ENST00000511181.5:c.-376-3767T>G	ENSP00000426285.1:n.-376-3767T>G
ENST00000513079.5:n.364+2T>G
ENST00000515528.1:n.354+2T>G
NM_000521.3:c.299+2T>G	NP_000512.1:n.299+2T>G
NM_001292004.1:c.-376-3767T>G	NP_001278933.1:n.-376-3767T>G
NM_000521.4:c.299+2T>G MANE Select	NP_000512.2:n.299+2T>G
NM_001292004.2:c.-376-3767T>G	NP_001278933.1:n.-376-3767T>G