Canonical Allele Identifier: CA400107669
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728257T>C , CM000679.2:g.48728257T>C GRCh38
NC_000017.10:g.46805619T>C , CM000679.1:g.46805619T>C GRCh37
NC_000017.9:g.44160618T>C NCBI36
NG_033789.1:g.5493A>G , LRG_771:g.5493A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.337A>G MANE Select ENSP00000290295.8:p.Thr113Ala
ENST00000290295.7:c.337A>G ENSP00000290295.7:p.Thr113Ala
NM_006361.5:c.337A>G , LRG_771t1:c.337A>G NP_006352.2:p.Thr113Ala
NM_006361.6:c.337A>G MANE Select NP_006352.2:p.Thr113Ala