Canonical Allele Identifier: CA1555781466
Gene: HEXB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74718749T= , CM000667.2:g.74718749T= GRCh38
NC_000005.9:g.74014574T= , CM000667.1:g.74014574T= GRCh37
NC_000005.8:g.74050330T= NCBI36
NG_009770.1:g.38606T=
NG_009770.2:g.83727T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.1243-48T= MANE Select ENSP00000261416.7:n.1243-48T=
ENST00000261416.11:c.1243-48T= ENSP00000261416.7:n.1243-48T=
ENST00000503312.5:c.119-48T=
ENST00000504459.5:n.440-48T=
ENST00000511181.5:c.568-48T= ENSP00000426285.1:n.568-48T=
ENST00000513336.5:c.179-48T=
ENST00000513539.1:n.74-160T=
NM_000521.3:c.1243-48T= NP_000512.1:n.1243-48T=
NM_001292004.1:c.568-48T= NP_001278933.1:n.568-48T=
NM_000521.4:c.1243-48T= MANE Select NP_000512.2:n.1243-48T=
NM_001292004.2:c.568-48T= NP_001278933.1:n.568-48T=