Canonical Allele Identifier: CA2581632422
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.86756774A>C , CM000668.2:g.86756774A>C GRCh38
NC_000006.11:g.87466492A>C , CM000668.1:g.87466492A>C GRCh37
NC_000006.10:g.87523211A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942749.1:n.531-26531T>G
XR_942750.1:n.511-26531T>G