Canonical Allele Identifier: CA658822550
Gene:

Linked Data

ClinVar Variation Id: 549922
ClinVar RCV Id: RCV000664502
dbSNP Id: rs1277208445
gnomAD v4: 11-5225432-G-T
MyVariant Identifiers: chr11:g.5246662G>T (hg19) chr11:g.5225432G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.5225432G>T , CM000673.2:g.5225432G>T GRCh38
NC_000011.9:g.5246662G>T , CM000673.1:g.5246662G>T GRCh37
NC_000011.8:g.5203238G>T NCBI36
NG_000007.3:g.72184C>A
NG_059281.1:g.6640C>A
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