Canonical Allele Identifier: CA572945091
Gene: STEAP1B HGNC NCBI

Linked Data

dbSNP Id: rs1201417839
gnomAD v2: 7-22756523-G-T
gnomAD v3: 7-22716904-G-T
gnomAD v4: 7-22716904-G-T
MyVariant Identifiers: chr7:g.22756523G>T (hg19) chr7:g.22716904G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.22716904G>T , CM000669.2:g.22716904G>T GRCh38
NC_000007.13:g.22756523G>T , CM000669.1:g.22756523G>T GRCh37
NC_000007.12:g.22723048G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650428.1:n.46+10664C>A
Search 100 bp 5'
Search 100 bp 3'