Canonical Allele Identifier: CA422484274
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769706T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800576T>A , CM000663.2:g.192800576T>A GRCh38
NC_000001.10:g.192769706T>A , CM000663.1:g.192769706T>A GRCh37
NC_000001.9:g.191036329T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.6T>A