Canonical Allele Identifier: CA500661881
Gene: HOXB13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.46805614G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48728252G>T , CM000679.2:g.48728252G>T GRCh38
NC_000017.10:g.46805614G>T , CM000679.1:g.46805614G>T GRCh37
NC_000017.9:g.44160613G>T NCBI36
NG_033789.1:g.5498C>A , LRG_771:g.5498C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000290295.8:c.342C>A MANE Select ENSP00000290295.8:p.Pro114=
ENST00000290295.7:c.342C>A ENSP00000290295.7:p.Pro114=
NM_006361.5:c.342C>A , LRG_771t1:c.342C>A NP_006352.2:p.Pro114=
NM_006361.6:c.342C>A MANE Select NP_006352.2:p.Pro114=