Canonical Allele Identifier: CA360062852
Gene: HEXB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74689331T>G , CM000667.2:g.74689331T>G GRCh38
NC_000005.9:g.73985156T>G , CM000667.1:g.73985156T>G GRCh37
NC_000005.8:g.74020912T>G NCBI36
NG_009770.1:g.9188T>G
NG_009770.2:g.54309T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.303T>G MANE Select ENSP00000261416.7:p.Tyr101Ter
ENST00000261416.11:c.303T>G ENSP00000261416.7:p.Tyr101Ter
ENST00000511181.5:c.-373T>G ENSP00000426285.1:n.-373T>G
ENST00000513079.5:n.368T>G
ENST00000515528.1:n.358T>G
NM_000521.3:c.303T>G NP_000512.1:p.Tyr101Ter
NM_001292004.1:c.-373T>G NP_001278933.1:n.-373T>G
NM_000521.4:c.303T>G MANE Select NP_000512.2:p.Tyr101Ter
NM_001292004.2:c.-373T>G NP_001278933.1:n.-373T>G