Canonical Allele Identifier: CA759215230

Gene:

Linked Data

• dbSNP Id: rs1289342090
• MyVariant Identifiers: chr2:g.1557822C>T (hg19) ; chr2:g.1554050C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1554050C>T , CM000664.2:g.1554050C>T	GRCh38
NC_000002.11:g.1557822C>T , CM000664.1:g.1557822C>T	GRCh37
NC_000002.10:g.1536829C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011510447.1:c.-1123C>T	XP_011508749.1:n.-1123C>T
XM_011510448.1:c.-1123C>T	XP_011508750.1:n.-1123C>T
XR_922720.1:n.85+2448G>A
XM_017005455.1:c.-1123C>T	XP_016860944.1:n.-1123C>T
NR_168373.1:n.746-120C>T