Canonical Allele Identifier: CA2674240532
Gene: HEXB HGNC NCBI

Linked Data

gnomAD v4: 5-74718743-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74718743T>G , CM000667.2:g.74718743T>G GRCh38
NC_000005.9:g.74014568T>G , CM000667.1:g.74014568T>G GRCh37
NC_000005.8:g.74050324T>G NCBI36
NG_009770.1:g.38600T>G
NG_009770.2:g.83721T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261416.12:c.1243-54T>G MANE Select ENSP00000261416.7:n.1243-54T>G
ENST00000261416.11:c.1243-54T>G ENSP00000261416.7:n.1243-54T>G
ENST00000503312.5:c.119-54T>G
ENST00000504459.5:n.440-54T>G
ENST00000511181.5:c.568-54T>G ENSP00000426285.1:n.568-54T>G
ENST00000513336.5:c.179-54T>G
ENST00000513539.1:n.74-166T>G
NM_000521.3:c.1243-54T>G NP_000512.1:n.1243-54T>G
NM_001292004.1:c.568-54T>G NP_001278933.1:n.568-54T>G
NM_000521.4:c.1243-54T>G MANE Select NP_000512.2:n.1243-54T>G
NM_001292004.2:c.568-54T>G NP_001278933.1:n.568-54T>G