Canonical Allele Identifier: CA185688699
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10086908

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999692T>C , CM000670.2:g.126999692T>C GRCh38
NC_000008.10:g.128011937T>C , CM000670.1:g.128011937T>C GRCh37
NC_000008.9:g.128081119T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6863T>C