Canonical Allele Identifier: CA124871238

Gene:

Linked Data

• dbSNP Id: rs11466734
• gnomAD v2: 5-110405628-T-C
• gnomAD v3: 5-111069930-T-C
• gnomAD v4: 5-111069930-T-C
• MyVariant Identifiers: chr5:g.110405628T>C (hg19) ; chr5:g.111069930T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.111069930T>C , CM000667.2:g.111069930T>C	GRCh38
NC_000005.9:g.110405628T>C , CM000667.1:g.110405628T>C	GRCh37
NC_000005.8:g.110433527T>C	NCBI36