Canonical Allele Identifier: CA755748349

Gene:

Linked Data

• dbSNP Id: rs1460795745
• MyVariant Identifiers: chr2:g.118837364A>G (hg19) ; chr2:g.118079788A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118079788A>G , CM000664.2:g.118079788A>G	GRCh38
NC_000002.11:g.118837364A>G , CM000664.1:g.118837364A>G	GRCh37
NC_000002.10:g.118553834A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011512305.1:c.697-2256T>C	XP_011510607.1:n.697-2256T>C
XR_001739662.2:n.138+8463T>C