Canonical Allele Identifier: CA1694134931
Gene: STEAP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22719806A= , CM000669.2:g.22719806A= GRCh38
NC_000007.13:g.22759425A= , CM000669.1:g.22759425A= GRCh37
NC_000007.12:g.22725950A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+7762T=