Canonical Allele Identifier: CA63405681

Gene:

Linked Data

• dbSNP Id: rs369151792
• MyVariant Identifiers: chr2:g.195871950C>A (hg19) ; chr2:g.195007226C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195007226C>A , CM000664.2:g.195007226C>A	GRCh38
NC_000002.11:g.195871950C>A , CM000664.1:g.195871950C>A	GRCh37
NC_000002.10:g.195580195C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001739836.1:n.553+52209G>T