Canonical Allele Identifier: CA3306128

Gene: HEXB

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74718982C>T , CM000667.2:g.74718982C>T	GRCh38
NC_000005.9:g.74014807C>T , CM000667.1:g.74014807C>T	GRCh37
NC_000005.8:g.74050563C>T	NCBI36
NG_009770.1:g.38839C>T
NG_009770.2:g.83960C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000521.4:c.1417+11C>T MANE Select	NP_000512.2:n.1417+11C>T
ENST00000261416.12:c.1417+11C>T MANE Select	ENSP00000261416.7:n.1417+11C>T
NM_000521.3:c.1417+11C>T	NP_000512.1:n.1417+11C>T
NM_001292004.1:c.742+11C>T	NP_001278933.1:n.742+11C>T
NM_001292004.2:c.742+11C>T	NP_001278933.1:n.742+11C>T
ENST00000261416.11:c.1417+11C>T	ENSP00000261416.7:n.1417+11C>T
ENST00000503312.5:c.293+11C>T
ENST00000504459.5:n.614+11C>T
ENST00000511181.5:c.742+11C>T	ENSP00000426285.1:n.742+11C>T
ENST00000513336.5:c.353+11C>T
ENST00000513539.1:n.136+11C>T