Canonical Allele Identifier: CA400107668
Gene: HOXB13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.46805619T>G (hg19) chr17:g.48728257T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728257T>G , CM000679.2:g.48728257T>G GRCh38
NC_000017.10:g.46805619T>G , CM000679.1:g.46805619T>G GRCh37
NC_000017.9:g.44160618T>G NCBI36
NG_033789.1:g.5493A>C , LRG_771:g.5493A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.337A>C MANE Select ENSP00000290295.8:p.Thr113Pro
ENST00000290295.7:c.337A>C ENSP00000290295.7:p.Thr113Pro
NM_006361.5:c.337A>C , LRG_771t1:c.337A>C NP_006352.2:p.Thr113Pro
NM_006361.6:c.337A>C MANE Select NP_006352.2:p.Thr113Pro
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