Canonical Allele Identifier: CA658796585
Gene:

Linked Data

ClinVar Variation Id: 537574
ClinVar RCV Id: RCV003538531
dbSNP Id: rs1554060097
MyVariant Identifiers: chr5:g.112043038G>C (hg19) chr5:g.112707341G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707341G>C , CM000667.2:g.112707341G>C GRCh38
NC_000005.9:g.112043038G>C , CM000667.1:g.112043038G>C GRCh37
NC_000005.8:g.112070937G>C NCBI36
NG_008481.4:g.19821G>C , LRG_130:g.19821G>C
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