Canonical Allele Identifier: CA422484623

Gene:

Linked Data

• dbSNP Id: rs1665422607
• MyVariant Identifiers: chr1:g.192769770T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.192800640T>C , CM000663.2:g.192800640T>C	GRCh38
NC_000001.10:g.192769770T>C , CM000663.1:g.192769770T>C	GRCh37
NC_000001.9:g.191036393T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000429211.2:n.70T>C