Canonical Allele Identifier: CA110736722

Gene:

Linked Data

• dbSNP Id: rs746134448
• gnomAD v2: 4-174515483-T-C
• gnomAD v3: 4-173594332-T-C
• gnomAD v4: 4-173594332-T-C
• MyVariant Identifiers: chr4:g.174515483T>C (hg19) ; chr4:g.173594332T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.173594332T>C , CM000666.2:g.173594332T>C	GRCh38
NC_000004.11:g.174515483T>C , CM000666.1:g.174515483T>C	GRCh37
NC_000004.10:g.174752058T>C	NCBI36