Canonical Allele Identifier: CA1649498158
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014570T= , CM000668.2:g.98014570T= GRCh38
NC_000006.11:g.98462446T= , CM000668.1:g.98462446T= GRCh37
NC_000006.10:g.98569167T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45104T=
XR_942809.1:n.371+45104T=