Canonical Allele Identifier: CA16155014
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.114229128T>C , CM000665.2:g.114229128T>C GRCh38
NC_000003.11:g.113947975T>C , CM000665.1:g.113947975T>C GRCh37
NC_000003.10:g.115430665T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001740856.1:n.161-4214T>C