Canonical Allele Identifier: CA1555781390

Gene: HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74718646G= , CM000667.2:g.74718646G=	GRCh38
NC_000005.9:g.74014471G= , CM000667.1:g.74014471G=	GRCh37
NC_000005.8:g.74050227G=	NCBI36
NG_009770.1:g.38503G=
NG_009770.2:g.83624G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261416.12:c.1243-151G= MANE Select	ENSP00000261416.7:n.1243-151G=
ENST00000261416.11:c.1243-151G=	ENSP00000261416.7:n.1243-151G=
ENST00000503312.5:c.119-151G=
ENST00000504459.5:n.440-151G=
ENST00000511181.5:c.568-151G=	ENSP00000426285.1:n.568-151G=
ENST00000513336.5:c.179-151G=
ENST00000513539.1:n.74-263G=
NM_000521.3:c.1243-151G=	NP_000512.1:n.1243-151G=
NM_001292004.1:c.568-151G=	NP_001278933.1:n.568-151G=
NM_000521.4:c.1243-151G= MANE Select	NP_000512.2:n.1243-151G=
NM_001292004.2:c.568-151G=	NP_001278933.1:n.568-151G=