Canonical Allele Identifier: CA2573138732
Gene:

Linked Data

ClinVar Variation Id: 1460838
ClinVar RCV Id: RCV003772962
dbSNP Id: rs2149627922
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707320C>A , CM000667.2:g.112707320C>A GRCh38
NC_000005.9:g.112043017C>A , CM000667.1:g.112043017C>A GRCh37
NC_000005.8:g.112070916C>A NCBI36
NG_008481.4:g.19800C>A , LRG_130:g.19800C>A
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