Canonical Allele Identifier: CA531201197

Gene:

Linked Data

• dbSNP Id: rs1206282157
• gnomAD v2: 2-15066110-A-G
• gnomAD v3: 2-14925986-A-G
• gnomAD v4: 2-14925986-A-G
• MyVariant Identifiers: chr2:g.15066110A>G (hg19) ; chr2:g.14925986A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.14925986A>G , CM000664.2:g.14925986A>G	GRCh38
NC_000002.11:g.15066110A>G , CM000664.1:g.15066110A>G	GRCh37
NC_000002.10:g.14983561A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_922818.1:n.205-146839T>C