Canonical Allele Identifier: CA1694135038
Gene: STEAP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22720015G= , CM000669.2:g.22720015G= GRCh38
NC_000007.13:g.22759634G= , CM000669.1:g.22759634G= GRCh37
NC_000007.12:g.22726159G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+7553C=