Canonical Allele Identifier: CA400107862
Gene: HOXB13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728354A>C , CM000679.2:g.48728354A>C GRCh38
NC_000017.10:g.46805716A>C , CM000679.1:g.46805716A>C GRCh37
NC_000017.9:g.44160715A>C NCBI36
NG_033789.1:g.5396T>G , LRG_771:g.5396T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000290295.8:c.240T>G MANE Select ENSP00000290295.8:p.Tyr80Ter
ENST00000290295.7:c.240T>G ENSP00000290295.7:p.Tyr80Ter
NM_006361.5:c.240T>G , LRG_771t1:c.240T>G NP_006352.2:p.Tyr80Ter
NM_006361.6:c.240T>G MANE Select NP_006352.2:p.Tyr80Ter