Canonical Allele Identifier: CA221875308
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs12365397

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.43214511A>G , CM000673.2:g.43214511A>G GRCh38
NC_000011.8:g.43192637A>G NCBI36
NC_000011.9:g.43236061A>G , CM000673.1:g.43236061A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000533565.1:n.129+54754T>C