ClinGen Allele Registry
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Canonical Allele Identifier:
CA155231221
Gene: STEAP1B
HGNC
NCBI
Linked Data
dbSNP Id:
rs917446288
MyVariant Identifiers:
chr7:g.22759467A>G (hg19)
chr7:g.22719848A>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22719848A>G , CM000669.2:g.22719848A>G
GRCh38
NC_000007.13:g.22759467A>G , CM000669.1:g.22759467A>G
GRCh37
NC_000007.12:g.22725992A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000650428.1:n.46+7720T>C
Search 100 bp 5'
Search 100 bp 3'