ClinGen Allele Registry
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Canonical Allele Identifier:
CA155231682
Gene: STEAP1B
HGNC
NCBI
Linked Data
dbSNP Id:
rs867476116
MyVariant Identifiers:
chr7:g.22759750C>T (hg19)
chr7:g.22720131C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22720131C>T , CM000669.2:g.22720131C>T
GRCh38
NC_000007.13:g.22759750C>T , CM000669.1:g.22759750C>T
GRCh37
NC_000007.12:g.22726275C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650428.1:n.46+7437G>A
Search 100 bp 5'
Search 100 bp 3'