Canonical Allele Identifier: CA561687862

Gene:

Linked Data

• dbSNP Id: rs1268100199
• gnomAD v2: 5-104207893-A-C
• gnomAD v3: 5-104872192-A-C
• gnomAD v4: 5-104872192-A-C
• MyVariant Identifiers: chr5:g.104207893A>C (hg19) ; chr5:g.104872192A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.104872192A>C , CM000667.2:g.104872192A>C	GRCh38
NC_000005.9:g.104207893A>C , CM000667.1:g.104207893A>C	GRCh37
NC_000005.8:g.104235792A>C	NCBI36