Canonical Allele Identifier: CA1573442262
Gene:

Linked Data

ClinVar Variation Id: 1020081
ClinVar RCV Id: RCV003538687
dbSNP Id: rs989021062
gnomAD v4: 5-112707408-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707408C>T , CM000667.2:g.112707408C>T GRCh38
NC_000005.9:g.112043105C>T , CM000667.1:g.112043105C>T GRCh37
NC_000005.8:g.112071004C>T NCBI36
NG_008481.4:g.19888C>T , LRG_130:g.19888C>T
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