Canonical Allele Identifier: CA43588557
Gene:

Linked Data

dbSNP Id: rs1034812677
MyVariant Identifiers: chr2:g.18025227A>C (hg19) chr2:g.17843960A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843960A>C , CM000664.2:g.17843960A>C GRCh38
NC_000002.11:g.18025227A>C , CM000664.1:g.18025227A>C GRCh37
NC_000002.10:g.17888708A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3734T>G
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