Canonical Allele Identifier: CA54648342

Gene:

Linked Data

• dbSNP Id: rs368226419
• MyVariant Identifiers: chr2:g.121089724G>A (hg19) ; chr2:g.120332148G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120332148G>A , CM000664.2:g.120332148G>A	GRCh38
NC_000002.11:g.121089724G>A , CM000664.1:g.121089724G>A	GRCh37
NC_000002.10:g.120806194G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011512307.1:c.141+3342G>A	XP_011510609.1:n.141+3342G>A