Canonical Allele Identifier: CA13404971
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs11223996

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134756993T>C , CM000673.2:g.134756993T>C GRCh38
NC_000011.9:g.134626887T>C , CM000673.1:g.134626887T>C GRCh37
NC_000011.8:g.134132097T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_147836.1:n.599-4081T>C