Canonical Allele Identifier: CA422484955

Gene:

Linked Data

• gnomAD v4: 1-192800714-A-G
• MyVariant Identifiers: chr1:g.192769844A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800714A>G , CM000663.2:g.192800714A>G	GRCh38
NC_000001.10:g.192769844A>G , CM000663.1:g.192769844A>G	GRCh37
NC_000001.9:g.191036467A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429211.2:n.144A>G