Canonical Allele Identifier: CA313510480

Gene:

Linked Data

• dbSNP Id: rs4911414
• gnomAD v2: 20-32729444-T-G
• gnomAD v3: 20-34141638-T-G
• gnomAD v4: 20-34141638-T-G
• MyVariant Identifiers: chr20:g.32729444T>G (hg19) ; chr20:g.34141638T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.34141638T>G , CM000682.2:g.34141638T>G	GRCh38
NC_000020.10:g.32729444T>G , CM000682.1:g.32729444T>G	GRCh37
NC_000020.9:g.32193105T>G	NCBI36