Canonical Allele Identifier: CA55082053

Gene:

Linked Data

• dbSNP Id: rs549443680
• MyVariant Identifiers: chr2:g.123641678C>T (hg19) ; chr2:g.122884102C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.122884102C>T , CM000664.2:g.122884102C>T	GRCh38
NC_000002.11:g.123641678C>T , CM000664.1:g.123641678C>T	GRCh37
NC_000002.10:g.123358148C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923292.1:n.1125-840C>T
XR_001739692.1:n.1451-840C>T
XR_923292.2:n.1358-840C>T