Canonical Allele Identifier: CA117655353

Gene:

Linked Data

• dbSNP Id: rs990135483
• gnomAD v2: 5-39979248-T-C
• gnomAD v3: 5-39979146-T-C
• gnomAD v4: 5-39979146-T-C
• MyVariant Identifiers: chr5:g.39979248T>C (hg19) ; chr5:g.39979146T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.39979146T>C , CM000667.2:g.39979146T>C	GRCh38
NC_000005.9:g.39979248T>C , CM000667.1:g.39979248T>C	GRCh37
NC_000005.8:g.40015005T>C	NCBI36