Canonical Allele Identifier: CA2824346482
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2789228C>G , CM000686.2:g.2789228C>G GRCh38
NC_000024.9:g.2657269C>G , CM000686.1:g.2657269C>G GRCh37
NC_000024.8:g.2717269C>G NCBI36
NG_011751.1:g.3524G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.106+14489C>G
ENST00000680285.1:n.320-521C>G
ENST00000681787.1:n.106+14489C>G
ENST00000681940.1:n.106+14489C>G