Canonical Allele Identifier: CA101676766

Gene:

Linked Data

• dbSNP Id: rs753991658
• gnomAD v2: 4-100274429-T-G
• gnomAD v3: 4-99353272-T-G
• gnomAD v4: 4-99353272-T-G
• MyVariant Identifiers: chr4:g.100274429T>G (hg19) ; chr4:g.99353272T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99353272T>G , CM000666.2:g.99353272T>G	GRCh38
NC_000004.11:g.100274429T>G , CM000666.1:g.100274429T>G	GRCh37
NC_000004.10:g.100493452T>G	NCBI36
NG_011718.1:g.4489A>C