Canonical Allele Identifier: CA755935312

Gene:

Linked Data

• dbSNP Id: rs1479499120
• gnomAD v3: 2-120332091-C-G
• gnomAD v4: 2-120332091-C-G
• MyVariant Identifiers: chr2:g.121089667C>G (hg19) ; chr2:g.120332091C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120332091C>G , CM000664.2:g.120332091C>G	GRCh38
NC_000002.11:g.121089667C>G , CM000664.1:g.121089667C>G	GRCh37
NC_000002.10:g.120806137C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011512307.1:c.141+3285C>G	XP_011510609.1:n.141+3285C>G