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Canonical Allele Identifier:
CA15521658
Gene: STEAP1B
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.22712807G>A
GRCh37
chr7:g.22752426G>A
Linked Data - Sequence & Population
gnomAD v2:
7:22752426 G / A
gnomAD v3:
7:22712807 G / A
gnomAD v4:
chr7-22712807-G-A
Joint Max Group AF
0.6164138 (EAS)
Genomes Max Group AF
0.6164138 (EAS)
Linked Data - NCBI & NCI
dbSNP:
6969502
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22712807G>A , CM000669.2:g.22712807G>A
GRCh38
NC_000007.13:g.22752426G>A , CM000669.1:g.22752426G>A
GRCh37
NC_000007.12:g.22718951G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650428.1:n.46+14761C>T
Search 100 bp 5'
Search 100 bp 3'