Canonical Allele Identifier: CA1318169387
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195006938C= , CM000664.2:g.195006938C= GRCh38
NC_000002.11:g.195871662C= , CM000664.1:g.195871662C= GRCh37
NC_000002.10:g.195579907C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52497G=