Canonical Allele Identifier: CA360062846

Gene: HEXB

Linked Data

• gnomAD v4: 5-74689329-T-C
• MyVariant Identifiers: chr5:g.73985154T>C (hg19) ; chr5:g.74689329T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74689329T>C , CM000667.2:g.74689329T>C	GRCh38
NC_000005.9:g.73985154T>C , CM000667.1:g.73985154T>C	GRCh37
NC_000005.8:g.74020910T>C	NCBI36
NG_009770.1:g.9186T>C
NG_009770.2:g.54307T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261416.12:c.301T>C MANE Select	ENSP00000261416.7:p.Tyr101His
ENST00000261416.11:c.301T>C	ENSP00000261416.7:p.Tyr101His
ENST00000511181.5:c.-375T>C	ENSP00000426285.1:n.-375T>C
ENST00000513079.5:n.366T>C
ENST00000515528.1:n.356T>C
NM_000521.3:c.301T>C	NP_000512.1:p.Tyr101His
NM_001292004.1:c.-375T>C	NP_001278933.1:n.-375T>C
NM_000521.4:c.301T>C MANE Select	NP_000512.2:p.Tyr101His
NM_001292004.2:c.-375T>C	NP_001278933.1:n.-375T>C