Canonical Allele Identifier: CA400107853
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728350A>G , CM000679.2:g.48728350A>G GRCh38
NC_000017.10:g.46805712A>G , CM000679.1:g.46805712A>G GRCh37
NC_000017.9:g.44160711A>G NCBI36
NG_033789.1:g.5400T>C , LRG_771:g.5400T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.244T>C MANE Select ENSP00000290295.8:p.Tyr82His
ENST00000290295.7:c.244T>C ENSP00000290295.7:p.Tyr82His
NM_006361.5:c.244T>C , LRG_771t1:c.244T>C NP_006352.2:p.Tyr82His
NM_006361.6:c.244T>C MANE Select NP_006352.2:p.Tyr82His