Canonical Allele Identifier: CA761272667

Gene:

Linked Data

• dbSNP Id: rs1261798677
• gnomAD v3: 2-17844076-T-G
• gnomAD v4: 2-17844076-T-G
• MyVariant Identifiers: chr2:g.18025343T>G (hg19) ; chr2:g.17844076T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.17844076T>G , CM000664.2:g.17844076T>G	GRCh38
NC_000002.11:g.18025343T>G , CM000664.1:g.18025343T>G	GRCh37
NC_000002.10:g.17888824T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_939764.2:n.447+3618A>C