Canonical Allele Identifier: CA400107657
Gene: HOXB13 HGNC NCBI

Linked Data

dbSNP Id: rs2143072711
MyVariant Identifiers: chr17:g.46805613T>A (hg19) chr17:g.48728251T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728251T>A , CM000679.2:g.48728251T>A GRCh38
NC_000017.10:g.46805613T>A , CM000679.1:g.46805613T>A GRCh37
NC_000017.9:g.44160612T>A NCBI36
NG_033789.1:g.5499A>T , LRG_771:g.5499A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.343A>T MANE Select ENSP00000290295.8:p.Thr115Ser
ENST00000290295.7:c.343A>T ENSP00000290295.7:p.Thr115Ser
NM_006361.5:c.343A>T , LRG_771t1:c.343A>T NP_006352.2:p.Thr115Ser
NM_006361.6:c.343A>T MANE Select NP_006352.2:p.Thr115Ser
Search 100 bp 5'
Search 100 bp 3'