Canonical Allele Identifier: CA1215982366
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800695G= , CM000663.2:g.192800695G= GRCh38
NC_000001.10:g.192769825G= , CM000663.1:g.192769825G= GRCh37
NC_000001.9:g.191036448G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.125G=