Canonical Allele Identifier: CA360062447
Gene: HEXB HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.73981341A>C (hg19) chr5:g.74685516A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.74685516A>C , CM000667.2:g.74685516A>C GRCh38
NC_000005.9:g.73981341A>C , CM000667.1:g.73981341A>C GRCh37
NC_000005.8:g.74017097A>C NCBI36
NG_009770.1:g.5373A>C
NG_009770.2:g.50494A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261416.12:c.256A>C MANE Select ENSP00000261416.7:p.Thr86Pro
ENST00000261416.11:c.256A>C ENSP00000261416.7:p.Thr86Pro
ENST00000511181.5:c.-376-3812A>C ENSP00000426285.1:n.-376-3812A>C
ENST00000513079.5:n.321A>C
ENST00000515528.1:n.311A>C
NM_000521.3:c.256A>C NP_000512.1:p.Thr86Pro
NM_001292004.1:c.-376-3812A>C NP_001278933.1:n.-376-3812A>C
NM_000521.4:c.256A>C MANE Select NP_000512.2:p.Thr86Pro
NM_001292004.2:c.-376-3812A>C NP_001278933.1:n.-376-3812A>C
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