ClinGen Allele Registry
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Canonical Allele Identifier:
CA836767854
Gene: STEAP1B
HGNC
NCBI
Linked Data
dbSNP Id:
rs545976608
MyVariant Identifiers:
chr7:g.22756505T>G (hg19)
chr7:g.22716886T>G (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.22716886T>G , CM000669.2:g.22716886T>G
GRCh38
NC_000007.13:g.22756505T>G , CM000669.1:g.22756505T>G
GRCh37
NC_000007.12:g.22723030T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid change
ENST00000650428.1:n.46+10682A>C
Search 100 bp 5'
Search 100 bp 3'