Canonical Allele Identifier: CA50218047
Gene:

Linked Data

dbSNP Id: rs937959857
MyVariant Identifiers: chr2:g.67864748A>C (hg19) chr2:g.67637616A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.67637616A>C , CM000664.2:g.67637616A>C GRCh38
NC_000002.11:g.67864748A>C , CM000664.1:g.67864748A>C GRCh37
NC_000002.10:g.67718252A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739524.1:n.65+13350T>G
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