Canonical Allele Identifier: CA756174249

Gene:

Linked Data

• dbSNP Id: rs1483390329
• MyVariant Identifiers: chr2:g.123126327C>T (hg19) ; chr2:g.122368751C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122368751C>T , CM000664.2:g.122368751C>T	GRCh38
NC_000002.11:g.123126327C>T , CM000664.1:g.123126327C>T	GRCh37
NC_000002.10:g.122842797C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923278.1:n.556-24212C>T
XR_001739684.1:n.556-24212C>T