Canonical Allele Identifier: CA836768435
Gene: STEAP1B HGNC NCBI

Linked Data

dbSNP Id: rs1254589477
MyVariant Identifiers: chr7:g.22760435G>A (hg19) chr7:g.22720816G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22720816G>A , CM000669.2:g.22720816G>A GRCh38
NC_000007.13:g.22760435G>A , CM000669.1:g.22760435G>A GRCh37
NC_000007.12:g.22726960G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+6752C>T
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