Canonical Allele Identifier: CA250073471
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs12430077

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52035072T>C , CM000675.2:g.52035072T>C GRCh38
NC_000013.9:g.51507209T>C NCBI36
NC_000013.10:g.52609208T>C , CM000675.1:g.52609208T>C GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000529080.5:n.2579A>G