Canonical Allele Identifier: CA12039379
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151020023T>C , CM000667.2:g.151020023T>C GRCh38
NC_000005.9:g.150399584T>C , CM000667.1:g.150399584T>C GRCh37
NC_000005.8:g.150379777T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944410.1:n.461A>G
XR_944410.2:n.307A>G