Canonical Allele Identifier: CA54965458

Gene:

Linked Data

• dbSNP Id: rs915954237
• MyVariant Identifiers: chr2:g.123126339C>T (hg19) ; chr2:g.122368763C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122368763C>T , CM000664.2:g.122368763C>T	GRCh38
NC_000002.11:g.123126339C>T , CM000664.1:g.123126339C>T	GRCh37
NC_000002.10:g.122842809C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-24200C>T
XR_001739684.1:n.556-24200C>T