Canonical Allele Identifier: CA400107665
Gene: HOXB13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.46805618G>A (hg19) chr17:g.48728256G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728256G>A , CM000679.2:g.48728256G>A GRCh38
NC_000017.10:g.46805618G>A , CM000679.1:g.46805618G>A GRCh37
NC_000017.9:g.44160617G>A NCBI36
NG_033789.1:g.5494C>T , LRG_771:g.5494C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.338C>T MANE Select ENSP00000290295.8:p.Thr113Ile
ENST00000290295.7:c.338C>T ENSP00000290295.7:p.Thr113Ile
NM_006361.5:c.338C>T , LRG_771t1:c.338C>T NP_006352.2:p.Thr113Ile
NM_006361.6:c.338C>T MANE Select NP_006352.2:p.Thr113Ile
Search 100 bp 5'
Search 100 bp 3'