Canonical Allele Identifier: CA31634938

Gene:

Linked Data

• dbSNP Id: rs867664695
• gnomAD v4: 1-161223698-T-C
• MyVariant Identifiers: chr1:g.161193488T>C (hg19) ; chr1:g.161223698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161223698T>C , CM000663.2:g.161223698T>C	GRCh38
NC_000001.10:g.161193488T>C , CM000663.1:g.161193488T>C	GRCh37
NC_000001.9:g.159460112T>C	NCBI36
NG_012043.1:g.4931A>G