Canonical Allele Identifier: CA1318169430
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006985G= , CM000664.2:g.195006985G= GRCh38
NC_000002.11:g.195871709G= , CM000664.1:g.195871709G= GRCh37
NC_000002.10:g.195579954G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52450C=