Canonical Allele Identifier: CA400107848
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728348G>T , CM000679.2:g.48728348G>T GRCh38
NC_000017.10:g.46805710G>T , CM000679.1:g.46805710G>T GRCh37
NC_000017.9:g.44160709G>T NCBI36
NG_033789.1:g.5402C>A , LRG_771:g.5402C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.246C>A MANE Select ENSP00000290295.8:p.Tyr82Ter
ENST00000290295.7:c.246C>A ENSP00000290295.7:p.Tyr82Ter
NM_006361.5:c.246C>A , LRG_771t1:c.246C>A NP_006352.2:p.Tyr82Ter
NM_006361.6:c.246C>A MANE Select NP_006352.2:p.Tyr82Ter