Canonical Allele Identifier: CA422484972
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769849A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800719A>T , CM000663.2:g.192800719A>T GRCh38
NC_000001.10:g.192769849A>T , CM000663.1:g.192769849A>T GRCh37
NC_000001.9:g.191036472A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.149A>T