Canonical Allele Identifier: CA422484477

Gene:

Linked Data

• dbSNP Id: rs1571640287
• MyVariant Identifiers: chr1:g.192769743T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800613T>G , CM000663.2:g.192800613T>G	GRCh38
NC_000001.10:g.192769743T>G , CM000663.1:g.192769743T>G	GRCh37
NC_000001.9:g.191036366T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000429211.2:n.43T>G