Canonical Allele Identifier: CA1215982339
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800598A= , CM000663.2:g.192800598A= GRCh38
NC_000001.10:g.192769728A= , CM000663.1:g.192769728A= GRCh37
NC_000001.9:g.191036351A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.28A=