Canonical Allele Identifier: CA422484953
Gene:

Linked Data

dbSNP Id: rs1665423259
MyVariant Identifiers: chr1:g.192769843G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800713G>A , CM000663.2:g.192800713G>A GRCh38
NC_000001.10:g.192769843G>A , CM000663.1:g.192769843G>A GRCh37
NC_000001.9:g.191036466G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.143G>A