Canonical Allele Identifier: CA422484717

Gene:

Linked Data

• gnomAD v4: 1-192800656-G-A
• MyVariant Identifiers: chr1:g.192769786G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800656G>A , CM000663.2:g.192800656G>A	GRCh38
NC_000001.10:g.192769786G>A , CM000663.1:g.192769786G>A	GRCh37
NC_000001.9:g.191036409G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429211.2:n.86G>A