Canonical Allele Identifier: CA1647465268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.93730886A>C , CM000668.2:g.93730886A>C GRCh38
NC_000006.11:g.94440604A>C , CM000668.1:g.94440604A>C GRCh37
NC_000006.10:g.94497325A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_015362.1:n.1869-5735A>C
NR_015362.2:n.1950-5735A>C
NR_152794.1:n.412-5735A>C
NR_152795.1:n.686-5735A>C