Canonical Allele Identifier: CA422484959
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769845T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800715T>C , CM000663.2:g.192800715T>C GRCh38
NC_000001.10:g.192769845T>C , CM000663.1:g.192769845T>C GRCh37
NC_000001.9:g.191036468T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.145T>C