Canonical Allele Identifier: CA35069266

Gene:

Linked Data

• dbSNP Id: rs1023862920
• MyVariant Identifiers: chr1:g.192769754A>G (hg19) ; chr1:g.192800624A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800624A>G , CM000663.2:g.192800624A>G	GRCh38
NC_000001.10:g.192769754A>G , CM000663.1:g.192769754A>G	GRCh37
NC_000001.9:g.191036377A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429211.2:n.54A>G