Canonical Allele Identifier: CA1083526037
Gene:

Linked Data

dbSNP Id: rs1324125310

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580997C>T , CM000667.2:g.159580997C>T GRCh38
NC_000005.9:g.159008004C>T , CM000667.1:g.159008004C>T GRCh37
NC_000005.8:g.158940582C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+562C>T
XR_941140.1:n.2075+562C>T
XR_941141.1:n.570+562C>T
XR_941139.2:n.2229+562C>T