Canonical Allele Identifier: CA836768483
Gene: STEAP1B HGNC NCBI

Linked Data

dbSNP Id: rs1367661027
gnomAD v3: 7-22721071-G-C
gnomAD v4: 7-22721071-G-C
MyVariant Identifiers: chr7:g.22760690G>C (hg19) chr7:g.22721071G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22721071G>C , CM000669.2:g.22721071G>C GRCh38
NC_000007.13:g.22760690G>C , CM000669.1:g.22760690G>C GRCh37
NC_000007.12:g.22727215G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+6497C>G
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