Canonical Allele Identifier: CA755935268

Gene:

Linked Data

• dbSNP Id: rs1230710444
• MyVariant Identifiers: chr2:g.121089578A>G (hg19) ; chr2:g.120332002A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120332002A>G , CM000664.2:g.120332002A>G	GRCh38
NC_000002.11:g.121089578A>G , CM000664.1:g.121089578A>G	GRCh37
NC_000002.10:g.120806048A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011512307.1:c.141+3196A>G	XP_011510609.1:n.141+3196A>G