Canonical Allele Identifier: CA836768418
Gene: STEAP1B HGNC NCBI

Linked Data

dbSNP Id: rs1293736655
gnomAD v3: 7-22720725-T-C
gnomAD v4: 7-22720725-T-C
MyVariant Identifiers: chr7:g.22760344T>C (hg19) chr7:g.22720725T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22720725T>C , CM000669.2:g.22720725T>C GRCh38
NC_000007.13:g.22760344T>C , CM000669.1:g.22760344T>C GRCh37
NC_000007.12:g.22726869T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+6843A>G
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