Canonical Allele Identifier: CA763204916

Gene:

Linked Data

• dbSNP Id: rs1282771006
• MyVariant Identifiers: chr2:g.200898102G>C (hg19) ; chr2:g.200033379G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033379G>C , CM000664.2:g.200033379G>C	GRCh38
NC_000002.11:g.200898102G>C , CM000664.1:g.200898102G>C	GRCh37
NC_000002.10:g.200606347G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22483C>G