ClinGen Allele Registry
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Canonical Allele Identifier:
CA155231488
Gene: STEAP1B
HGNC
NCBI
Linked Data
dbSNP Id:
rs887882632
gnomAD v2:
7-22759635-T-G
gnomAD v3:
7-22720016-T-G
gnomAD v4:
7-22720016-T-G
MyVariant Identifiers:
chr7:g.22759635T>G (hg19)
chr7:g.22720016T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22720016T>G , CM000669.2:g.22720016T>G
GRCh38
NC_000007.13:g.22759635T>G , CM000669.1:g.22759635T>G
GRCh37
NC_000007.12:g.22726160T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650428.1:n.46+7552A>C
Search 100 bp 5'
Search 100 bp 3'