Canonical Allele Identifier: CA1694135029
Gene: STEAP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22719993A= , CM000669.2:g.22719993A= GRCh38
NC_000007.13:g.22759612A= , CM000669.1:g.22759612A= GRCh37
NC_000007.12:g.22726137A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650428.1:n.46+7575T=