Canonical Allele Identifier: CA1318169522
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007182A= , CM000664.2:g.195007182A= GRCh38
NC_000002.11:g.195871906A= , CM000664.1:g.195871906A= GRCh37
NC_000002.10:g.195580151A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52253T=