Canonical Allele Identifier: CA400107849
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728349T>A , CM000679.2:g.48728349T>A GRCh38
NC_000017.10:g.46805711T>A , CM000679.1:g.46805711T>A GRCh37
NC_000017.9:g.44160710T>A NCBI36
NG_033789.1:g.5401A>T , LRG_771:g.5401A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.245A>T MANE Select ENSP00000290295.8:p.Tyr82Phe
ENST00000290295.7:c.245A>T ENSP00000290295.7:p.Tyr82Phe
NM_006361.5:c.245A>T , LRG_771t1:c.245A>T NP_006352.2:p.Tyr82Phe
NM_006361.6:c.245A>T MANE Select NP_006352.2:p.Tyr82Phe