Canonical Allele Identifier: CA15094498

Gene:

Linked Data

• dbSNP Id: rs689466
• gnomAD v2: 1-186650751-T-C
• gnomAD v3: 1-186681619-T-C
• gnomAD v4: 1-186681619-T-C
• MyVariant Identifiers: chr1:g.186650751T>C (hg19) ; chr1:g.186681619T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.186681619T>C , CM000663.2:g.186681619T>C	GRCh38
NC_000001.10:g.186650751T>C , CM000663.1:g.186650751T>C	GRCh37
NC_000001.9:g.184917374T>C	NCBI36
NG_028206.2:g.3809A>G