Canonical Allele Identifier: CA1263130932
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.77848118G= , CM000664.2:g.77848118G= GRCh38
NC_000002.11:g.78075244G= , CM000664.1:g.78075244G= GRCh37
NC_000002.10:g.77928752G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110288.1:n.428-8228C=