Canonical Allele Identifier: CA34407162

Gene:

Linked Data

• dbSNP Id: rs1001523322
• gnomAD v4: 1-193121712-G-A
• MyVariant Identifiers: chr1:g.193090842G>A (hg19) ; chr1:g.193121712G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.193121712G>A , CM000663.2:g.193121712G>A	GRCh38
NC_000001.10:g.193090842G>A , CM000663.1:g.193090842G>A	GRCh37
NC_000001.9:g.191357465G>A	NCBI36
NG_012691.1:g.4755G>A , LRG_507:g.4755G>A

Transcript Alleles

HGVS	Amino-acid Change
XR_001738350.1:n.1945C>T