Canonical Allele Identifier: CA123949747

Gene:

Linked Data

• dbSNP Id: rs449650
• gnomAD v2: 5-99949018-T-G
• gnomAD v3: 5-100613314-T-G
• gnomAD v4: 5-100613314-T-G
• MyVariant Identifiers: chr5:g.99949018T>G (hg19) ; chr5:g.100613314T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.100613314T>G , CM000667.2:g.100613314T>G	GRCh38
NC_000005.9:g.99949018T>G , CM000667.1:g.99949018T>G	GRCh37
NC_000005.8:g.99976917T>G	NCBI36