Canonical Allele Identifier: CA2674237933

Gene: HEXB

Linked Data

• gnomAD v4: 5-74689193-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74689193G>T , CM000667.2:g.74689193G>T	GRCh38
NC_000005.9:g.73985018G>T , CM000667.1:g.73985018G>T	GRCh37
NC_000005.8:g.74020774G>T	NCBI36
NG_009770.1:g.9050G>T
NG_009770.2:g.54171G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261416.12:c.300-135G>T MANE Select	ENSP00000261416.7:n.300-135G>T
ENST00000261416.11:c.300-135G>T	ENSP00000261416.7:n.300-135G>T
ENST00000511181.5:c.-376-135G>T	ENSP00000426285.1:n.-376-135G>T
ENST00000513079.5:n.365-135G>T
ENST00000515528.1:n.355-135G>T
NM_000521.3:c.300-135G>T	NP_000512.1:n.300-135G>T
NM_001292004.1:c.-376-135G>T	NP_001278933.1:n.-376-135G>T
NM_000521.4:c.300-135G>T MANE Select	NP_000512.2:n.300-135G>T
NM_001292004.2:c.-376-135G>T	NP_001278933.1:n.-376-135G>T