Canonical Allele Identifier: CA422484917
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769832G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800702G>A , CM000663.2:g.192800702G>A GRCh38
NC_000001.10:g.192769832G>A , CM000663.1:g.192769832G>A GRCh37
NC_000001.9:g.191036455G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.132G>A