Canonical Allele Identifier: CA360070180

Gene: HEXB

Linked Data

• gnomAD v4: 5-74718809-A-G
• MyVariant Identifiers: chr5:g.74014634A>G (hg19) ; chr5:g.74718809A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.74718809A>G , CM000667.2:g.74718809A>G	GRCh38
NC_000005.9:g.74014634A>G , CM000667.1:g.74014634A>G	GRCh37
NC_000005.8:g.74050390A>G	NCBI36
NG_009770.1:g.38666A>G
NG_009770.2:g.83787A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261416.12:c.1255A>G MANE Select	ENSP00000261416.7:p.Thr419Ala
ENST00000261416.11:c.1255A>G	ENSP00000261416.7:p.Thr419Ala
ENST00000503312.5:c.131A>G
ENST00000504459.5:n.452A>G
ENST00000511181.5:c.580A>G	ENSP00000426285.1:p.Thr194Ala
ENST00000513336.5:c.191A>G
ENST00000513539.1:n.74-100A>G
NM_000521.3:c.1255A>G	NP_000512.1:p.Thr419Ala
NM_001292004.1:c.580A>G	NP_001278933.1:p.Thr194Ala
NM_000521.4:c.1255A>G MANE Select	NP_000512.2:p.Thr419Ala
NM_001292004.2:c.580A>G	NP_001278933.1:p.Thr194Ala