Canonical Allele Identifier: CA400107679
Gene: HOXB13 HGNC NCBI

Linked Data

dbSNP Id: rs781117900
MyVariant Identifiers: chr17:g.46805624G>C (hg19) chr17:g.48728262G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728262G>C , CM000679.2:g.48728262G>C GRCh38
NC_000017.10:g.46805624G>C , CM000679.1:g.46805624G>C GRCh37
NC_000017.9:g.44160623G>C NCBI36
NG_033789.1:g.5488C>G , LRG_771:g.5488C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.332C>G MANE Select ENSP00000290295.8:p.Ala111Gly
ENST00000290295.7:c.332C>G ENSP00000290295.7:p.Ala111Gly
NM_006361.5:c.332C>G , LRG_771t1:c.332C>G NP_006352.2:p.Ala111Gly
NM_006361.6:c.332C>G MANE Select NP_006352.2:p.Ala111Gly
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