Canonical Allele Identifier: CA756215017

Gene:

Linked Data

• dbSNP Id: rs1166638997
• MyVariant Identifiers: chr2:g.123641696G>C (hg19) ; chr2:g.122884120G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122884120G>C , CM000664.2:g.122884120G>C	GRCh38
NC_000002.11:g.123641696G>C , CM000664.1:g.123641696G>C	GRCh37
NC_000002.10:g.123358166G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-822G>C
XR_001739692.1:n.1451-822G>C
XR_923292.2:n.1358-822G>C