Canonical Allele Identifier: CA63405665

Gene:

Linked Data

• dbSNP Id: rs1044989798
• MyVariant Identifiers: chr2:g.195871766C>T (hg19) ; chr2:g.195007042C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.195007042C>T , CM000664.2:g.195007042C>T	GRCh38
NC_000002.11:g.195871766C>T , CM000664.1:g.195871766C>T	GRCh37
NC_000002.10:g.195580011C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001739836.1:n.553+52393G>A