Canonical Allele Identifier: CA400107838
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728344C>A , CM000679.2:g.48728344C>A GRCh38
NC_000017.10:g.46805706C>A , CM000679.1:g.46805706C>A GRCh37
NC_000017.9:g.44160705C>A NCBI36
NG_033789.1:g.5406G>T , LRG_771:g.5406G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.250G>T MANE Select ENSP00000290295.8:p.Gly84Ter
ENST00000290295.7:c.250G>T ENSP00000290295.7:p.Gly84Ter
NM_006361.5:c.250G>T , LRG_771t1:c.250G>T NP_006352.2:p.Gly84Ter
NM_006361.6:c.250G>T MANE Select NP_006352.2:p.Gly84Ter