Canonical Allele Identifier: CA476175291
Gene:

Linked Data

MyVariant Identifiers: chr11:g.89466632C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89733464C>G , CM000673.2:g.89733464C>G GRCh38
NC_000011.9:g.89466632C>G , CM000673.1:g.89466632C>G GRCh37
NC_000011.8:g.89106280C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000527668.1:n.2448C>G