Canonical Allele Identifier: CA116349001

Gene:

Linked Data

• dbSNP Id: rs1025145685
• gnomAD v2: 5-28339992-T-C
• gnomAD v3: 5-28339885-T-C
• gnomAD v4: 5-28339885-T-C
• MyVariant Identifiers: chr5:g.28339992T>C (hg19) ; chr5:g.28339885T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.28339885T>C , CM000667.2:g.28339885T>C	GRCh38
NC_000005.9:g.28339992T>C , CM000667.1:g.28339992T>C	GRCh37
NC_000005.8:g.28375749T>C	NCBI36