Canonical Allele Identifier: CA2552777622
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98102541A>T , CM000668.2:g.98102541A>T GRCh38
NC_000006.11:g.98550417A>T , CM000668.1:g.98550417A>T GRCh37
NC_000006.10:g.98657138A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_245563.2:n.456+3271A>T
XR_942809.1:n.456+3271A>T