Canonical Allele Identifier: CA112918836

Gene:

Linked Data

• dbSNP Id: rs146901406
• gnomAD v2: 5-1249635-A-T
• gnomAD v3: 5-1249520-A-T
• gnomAD v4: 5-1249520-A-T
• MyVariant Identifiers: chr5:g.1249635A>T (hg19) ; chr5:g.1249520A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1249520A>T , CM000667.2:g.1249520A>T	GRCh38
NC_000005.9:g.1249635A>T , CM000667.1:g.1249635A>T	GRCh37
NC_000005.8:g.1302635A>T	NCBI36