Canonical Allele Identifier: CA346233207

Gene:

Linked Data

• dbSNP Id: rs763267606
• MyVariant Identifiers: chr2:g.20685472G>A (hg19) ; chr2:g.20485711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20485711G>A , CM000664.2:g.20485711G>A	GRCh38
NC_000002.11:g.20685472G>A , CM000664.1:g.20685472G>A	GRCh37
NC_000002.10:g.20548953G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_157978.1:n.530+3027C>T