Canonical Allele Identifier: CA2824346739
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2800311A>G , CM000686.2:g.2800311A>G GRCh38
NC_000024.9:g.2668352A>G , CM000686.1:g.2668352A>G GRCh37
NC_000024.8:g.2728352A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+25572A>G
ENST00000681787.1:n.106+25572A>G
ENST00000681940.1:n.106+25572A>G