Canonical Allele Identifier: CA113485219

Gene:

Linked Data

• dbSNP Id: rs1001249071
• gnomAD v2: 5-4029563-A-C
• gnomAD v3: 5-4029450-A-C
• gnomAD v4: 5-4029450-A-C
• MyVariant Identifiers: chr5:g.4029563A>C (hg19) ; chr5:g.4029563_4029564delinsCC (hg19) ; chr5:g.4029450A>C (hg38) ; chr5:g.4029450_4029451delinsCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.4029450A>C , CM000667.2:g.4029450A>C	GRCh38
NC_000005.9:g.4029563A>C , CM000667.1:g.4029563A>C	GRCh37
NC_000005.8:g.4082563A>C	NCBI36