Canonical Allele Identifier: CA763641371

Gene:

Linked Data

• dbSNP Id: rs1353967007
• MyVariant Identifiers: chr2:g.20685406C>T (hg19) ; chr2:g.20485645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.20485645C>T , CM000664.2:g.20485645C>T	GRCh38
NC_000002.11:g.20685406C>T , CM000664.1:g.20685406C>T	GRCh37
NC_000002.10:g.20548887C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_157978.1:n.530+3093G>A