Canonical Allele Identifier: CA209782071
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs12261589

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.77781077C>T , CM000672.2:g.77781077C>T GRCh38
NC_000010.10:g.79540835C>T , CM000672.1:g.79540835C>T GRCh37
NC_000010.9:g.79210841C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439688.1:n.800G>A