Canonical Allele Identifier: CA1555776625

Gene: HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74685510A= , CM000667.2:g.74685510A=	GRCh38
NC_000005.9:g.73981335A= , CM000667.1:g.73981335A=	GRCh37
NC_000005.8:g.74017091A=	NCBI36
NG_009770.1:g.5367A=
NG_009770.2:g.50488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261416.12:c.250A= MANE Select	ENSP00000261416.7:p.Asn84=
ENST00000261416.11:c.250A=	ENSP00000261416.7:p.Asn84=
ENST00000511181.5:c.-376-3818A=	ENSP00000426285.1:n.-376-3818A=
ENST00000513079.5:n.315A=
ENST00000515528.1:n.305A=
NM_000521.3:c.250A=	NP_000512.1:p.Asn84=
NM_001292004.1:c.-376-3818A=	NP_001278933.1:n.-376-3818A=
NM_000521.4:c.250A= MANE Select	NP_000512.2:p.Asn84=
NM_001292004.2:c.-376-3818A=	NP_001278933.1:n.-376-3818A=