Canonical Allele Identifier: CA2541146730
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439757T>G , CM000668.2:g.31439757T>G GRCh38
NC_000006.11:g.31407534T>G , CM000668.1:g.31407534T>G GRCh37
NC_000006.10:g.31515513T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.350A>C