Canonical Allele Identifier: CA765624949

Gene:

Linked Data

• dbSNP Id: rs1168639656
• MyVariant Identifiers: chr2:g.227020711T>C (hg19) ; chr2:g.226155995T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.226155995T>C , CM000664.2:g.226155995T>C	GRCh38
NC_000002.11:g.227020711T>C , CM000664.1:g.227020711T>C	GRCh37
NC_000002.10:g.226728955T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046102.1:n.293-8393T>C