Canonical Allele Identifier: CA2540183181
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633397T>C , CM000668.2:g.151633397T>C GRCh38
NC_000006.11:g.151954532T>C , CM000668.1:g.151954532T>C GRCh37
NC_000006.10:g.151996225T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3415T>C