Canonical Allele Identifier: CA113505943

Gene:

Linked Data

• dbSNP Id: rs900347634
• gnomAD v2: 5-4196128-T-C
• gnomAD v3: 5-4196015-T-C
• gnomAD v4: 5-4196015-T-C
• MyVariant Identifiers: chr5:g.4196128T>C (hg19) ; chr5:g.4196015T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.4196015T>C , CM000667.2:g.4196015T>C	GRCh38
NC_000005.9:g.4196128T>C , CM000667.1:g.4196128T>C	GRCh37
NC_000005.8:g.4249128T>C	NCBI36