Canonical Allele Identifier: CA756215032

Gene:

Linked Data

• dbSNP Id: rs1375391967
• MyVariant Identifiers: chr2:g.123641769A>G (hg19) ; chr2:g.122884193A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122884193A>G , CM000664.2:g.122884193A>G	GRCh38
NC_000002.11:g.123641769A>G , CM000664.1:g.123641769A>G	GRCh37
NC_000002.10:g.123358239A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-749A>G
XR_001739692.1:n.1451-749A>G
XR_923292.2:n.1358-749A>G