Canonical Allele Identifier: CA31677619

Gene:

Linked Data

• dbSNP Id: rs1006127751
• gnomAD v2: 1-161184728-C-T
• gnomAD v3: 1-161214938-C-T
• gnomAD v4: 1-161214938-C-T
• MyVariant Identifiers: chr1:g.161184728C>T (hg19) ; chr1:g.161214938C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161214938C>T , CM000663.2:g.161214938C>T	GRCh38
NC_000001.10:g.161184728C>T , CM000663.1:g.161184728C>T	GRCh37
NC_000001.9:g.159451352C>T	NCBI36
NG_013352.1:g.20624C>T
NG_029043.1:g.4642C>T