Canonical Allele Identifier: CA1694135013
Gene: STEAP1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22719971T= , CM000669.2:g.22719971T= GRCh38
NC_000007.13:g.22759590T= , CM000669.1:g.22759590T= GRCh37
NC_000007.12:g.22726115T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+7597A=