Canonical Allele Identifier: CA54966620

Gene:

Linked Data

• dbSNP Id: rs899506182
• MyVariant Identifiers: chr2:g.123136844C>A (hg19) ; chr2:g.122379268C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122379268C>A , CM000664.2:g.122379268C>A	GRCh38
NC_000002.11:g.123136844C>A , CM000664.1:g.123136844C>A	GRCh37
NC_000002.10:g.122853314C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-13695C>A
XR_001739684.1:n.556-13695C>A