Canonical Allele Identifier: CA400107659
Gene: HOXB13 HGNC NCBI

Linked Data

dbSNP Id: rs2143072711

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728251T>G , CM000679.2:g.48728251T>G GRCh38
NC_000017.10:g.46805613T>G , CM000679.1:g.46805613T>G GRCh37
NC_000017.9:g.44160612T>G NCBI36
NG_033789.1:g.5499A>C , LRG_771:g.5499A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.343A>C MANE Select ENSP00000290295.8:p.Thr115Pro
ENST00000290295.7:c.343A>C ENSP00000290295.7:p.Thr115Pro
NM_006361.5:c.343A>C , LRG_771t1:c.343A>C NP_006352.2:p.Thr115Pro
NM_006361.6:c.343A>C MANE Select NP_006352.2:p.Thr115Pro