Canonical Allele Identifier: CA11973172
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs13358260

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79549888T>C , CM000667.2:g.79549888T>C GRCh38
NC_000005.8:g.78881467T>C NCBI36
NC_000005.9:g.78845711T>C , CM000667.1:g.78845711T>C GRCh37

Transcript Alleles

HGVS Amino-acid change
XR_948497.1:n.72+2244T>C
XR_948498.1:n.159+2051T>C
XR_948499.1:n.67+1586T>C