Canonical Allele Identifier: CA59498029
Gene:

Linked Data

dbSNP Id: rs1003517476
gnomAD v3: 2-160900663-T-C
gnomAD v4: 2-160900663-T-C
MyVariant Identifiers: chr2:g.161757174T>C (hg19) chr2:g.160900663T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.160900663T>C , CM000664.2:g.160900663T>C GRCh38
NC_000002.11:g.161757174T>C , CM000664.1:g.161757174T>C GRCh37
NC_000002.10:g.161465420T>C NCBI36
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