Canonical Allele Identifier: CA1649498229
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98014664T= , CM000668.2:g.98014664T= GRCh38
NC_000006.11:g.98462540T= , CM000668.1:g.98462540T= GRCh37
NC_000006.10:g.98569261T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.371+45198T=
XR_942809.1:n.371+45198T=