Canonical Allele Identifier: CA360062397

Gene: HEXB

Linked Data

• MyVariant Identifiers: chr5:g.73981319C>G (hg19) ; chr5:g.74685494C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74685494C>G , CM000667.2:g.74685494C>G	GRCh38
NC_000005.9:g.73981319C>G , CM000667.1:g.73981319C>G	GRCh37
NC_000005.8:g.74017075C>G	NCBI36
NG_009770.1:g.5351C>G
NG_009770.2:g.50472C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261416.12:c.234C>G MANE Select	ENSP00000261416.7:p.Tyr78Ter
ENST00000261416.11:c.234C>G	ENSP00000261416.7:p.Tyr78Ter
ENST00000511181.5:c.-376-3834C>G	ENSP00000426285.1:n.-376-3834C>G
ENST00000513079.5:n.299C>G
ENST00000515528.1:n.289C>G
NM_000521.3:c.234C>G	NP_000512.1:p.Tyr78Ter
NM_001292004.1:c.-376-3834C>G	NP_001278933.1:n.-376-3834C>G
NM_000521.4:c.234C>G MANE Select	NP_000512.2:p.Tyr78Ter
NM_001292004.2:c.-376-3834C>G	NP_001278933.1:n.-376-3834C>G