Canonical Allele Identifier: CA2504389859
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633493G>T , CM000668.2:g.151633493G>T GRCh38
NC_000006.11:g.151954628G>T , CM000668.1:g.151954628G>T GRCh37
NC_000006.10:g.151996321G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3511G>T