Canonical Allele Identifier: CA422484921
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769833C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800703C>T , CM000663.2:g.192800703C>T GRCh38
NC_000001.10:g.192769833C>T , CM000663.1:g.192769833C>T GRCh37
NC_000001.9:g.191036456C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.133C>T