Canonical Allele Identifier: CA55082031

Gene:

Linked Data

• dbSNP Id: rs114242038
• MyVariant Identifiers: chr2:g.123641527C>G (hg19) ; chr2:g.122883951C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122883951C>G , CM000664.2:g.122883951C>G	GRCh38
NC_000002.11:g.123641527C>G , CM000664.1:g.123641527C>G	GRCh37
NC_000002.10:g.123357997C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-991C>G
XR_001739692.1:n.1451-991C>G
XR_923292.2:n.1358-991C>G