Canonical Allele Identifier: CA513685612
Gene:

Linked Data

dbSNP Id: rs1924848063
gnomAD v4: 22-23573080-G-A
MyVariant Identifiers: chr22:g.23915267G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573080G>A , CM000684.2:g.23573080G>A GRCh38
NC_000022.10:g.23915267G>A , CM000684.1:g.23915267G>A GRCh37
NC_000022.9:g.22245267G>A NCBI36
NG_009791.1:g.12229C>T , LRG_69:g.12229C>T

Transcript Alleles

HGVS Amino-acid Change
XR_938078.1:n.685G>A
XR_938078.2:n.1269G>A
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