Canonical Allele Identifier: CA1555779288

Gene: HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74689106T= , CM000667.2:g.74689106T=	GRCh38
NC_000005.9:g.73984931T= , CM000667.1:g.73984931T=	GRCh37
NC_000005.8:g.74020687T=	NCBI36
NG_009770.1:g.8963T=
NG_009770.2:g.54084T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261416.12:c.300-222T= MANE Select	ENSP00000261416.7:n.300-222T=
ENST00000261416.11:c.300-222T=	ENSP00000261416.7:n.300-222T=
ENST00000511181.5:c.-376-222T=	ENSP00000426285.1:n.-376-222T=
ENST00000513079.5:n.365-222T=
ENST00000515528.1:n.355-222T=
NM_000521.3:c.300-222T=	NP_000512.1:n.300-222T=
NM_001292004.1:c.-376-222T=	NP_001278933.1:n.-376-222T=
NM_000521.4:c.300-222T= MANE Select	NP_000512.2:n.300-222T=
NM_001292004.2:c.-376-222T=	NP_001278933.1:n.-376-222T=