Canonical Allele Identifier: CA500661888
Gene: HOXB13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.46805617A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728255A>G , CM000679.2:g.48728255A>G GRCh38
NC_000017.10:g.46805617A>G , CM000679.1:g.46805617A>G GRCh37
NC_000017.9:g.44160616A>G NCBI36
NG_033789.1:g.5495T>C , LRG_771:g.5495T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.339T>C MANE Select ENSP00000290295.8:p.Thr113=
ENST00000290295.7:c.339T>C ENSP00000290295.7:p.Thr113=
NM_006361.5:c.339T>C , LRG_771t1:c.339T>C NP_006352.2:p.Thr113=
NM_006361.6:c.339T>C MANE Select NP_006352.2:p.Thr113=
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Search 100 bp 3'