Canonical Allele Identifier: CA8631759
Gene: HOXB1 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.48530455C>T , CM000679.2:g.48530455C>T GRCh38
NC_000017.10:g.46607817C>T , CM000679.1:g.46607817C>T GRCh37
NC_000017.9:g.43962816C>T NCBI36
NG_032884.1:g.5456G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000239174.7:c.450G>A MANE Select ENSP00000355140.5:p.Ala150=
ENST00000239174.6:c.450G>A ENSP00000355140.5:p.Ala150=
ENST00000577092.1:c.450G>A ENSP00000459066.1:p.Ala150=
NM_002144.3:c.450G>A NP_002135.2:p.Ala150=
NM_002144.4:c.450G>A MANE Select NP_002135.2:p.Ala150=