Canonical Allele Identifier: CA16365585
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.82521969A>G , CM000671.2:g.82521969A>G GRCh38
NC_000009.11:g.85136884A>G , CM000671.1:g.85136884A>G GRCh37
NC_000009.10:g.84326704A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000589973.2:n.247+25111A>G
ENST00000590298.5:n.440-42060A>G
ENST00000590791.5:n.526-2550A>G
ENST00000591257.5:n.347-2550A>G
ENST00000637606.1:n.985+25111A>G
XR_001746782.1:n.241+25111A>G