Canonical Allele Identifier: CA124924708
Gene:

Linked Data

ClinVar Variation Id: 469869
ClinVar RCV Id: RCV003742657
dbSNP Id: rs931845291
gnomAD v2: 5-112043163-T-C
gnomAD v3: 5-112707466-T-C
gnomAD v4: 5-112707466-T-C
MyVariant Identifiers: chr5:g.112043163T>C (hg19) chr5:g.112707466T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707466T>C , CM000667.2:g.112707466T>C GRCh38
NC_000005.9:g.112043163T>C , CM000667.1:g.112043163T>C GRCh37
NC_000005.8:g.112071062T>C NCBI36
NG_008481.4:g.19946T>C , LRG_130:g.19946T>C
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