Canonical Allele Identifier: CA2832690088
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8525169A>G , CM000668.2:g.8525169A>G GRCh38
NC_000006.11:g.8525402A>G , CM000668.1:g.8525402A>G GRCh37
NC_000006.10:g.8470401A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038979.1:n.626-33416A>G
NR_038980.1:n.649-33416A>G