Canonical Allele Identifier: CA2809312577
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35880795G>C , CM000679.2:g.35880795G>C GRCh38
NC_000017.9:g.31231912G>C NCBI36
NG_015990.1:g.4579C>G

Transcript Alleles

HGVS Amino-acid Change
XR_934696.1:n.197-3587G>C
XR_934697.1:n.200-3587G>C
XR_001752852.1:n.426+721G>C
XR_934696.2:n.91-3587G>C
XR_934697.2:n.91-3587G>C