Canonical Allele Identifier: CA422484722

Gene:

Linked Data

• MyVariant Identifiers: chr1:g.192769787T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800657T>G , CM000663.2:g.192800657T>G	GRCh38
NC_000001.10:g.192769787T>G , CM000663.1:g.192769787T>G	GRCh37
NC_000001.9:g.191036410T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429211.2:n.87T>G