Canonical Allele Identifier: CA64382955

Gene:

Linked Data

• dbSNP Id: rs1046052693
• MyVariant Identifiers: chr2:g.200033374C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033374C>A , CM000664.2:g.200033374C>A	GRCh38
NC_000002.11:g.200898097C>A , CM000664.1:g.200898097C>A	GRCh37
NC_000002.10:g.200606342C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22478G>T