Canonical Allele Identifier: CA2760462807
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578262A>T , CM000666.2:g.12578262A>T GRCh38
NC_000004.11:g.12579886A>T , CM000666.1:g.12579886A>T GRCh37
NC_000004.10:g.12188984A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31080T>A
XR_001741374.1:n.254+44393T>A
XR_925406.3:n.140+31080T>A