Canonical Allele Identifier: CA422484454

Gene:

Linked Data

• gnomAD v4: 1-192800608-C-G
• MyVariant Identifiers: chr1:g.192769738C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800608C>G , CM000663.2:g.192800608C>G	GRCh38
NC_000001.10:g.192769738C>G , CM000663.1:g.192769738C>G	GRCh37
NC_000001.9:g.191036361C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429211.2:n.38C>G