Canonical Allele Identifier: CA13610781
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.1529005A>G , CM000674.2:g.1529005A>G GRCh38
NC_000012.11:g.1638171A>G , CM000674.1:g.1638171A>G GRCh37
NC_000012.10:g.1508432A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017020292.2:c.*835T>C XP_016875781.1:n.*835T>C
NR_160736.1:n.2854T>C