Canonical Allele Identifier: CA1557963327
Gene:

Linked Data

dbSNP Id: rs1753644537

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.79549823A>G , CM000667.2:g.79549823A>G GRCh38
NC_000005.9:g.78845646A>G , CM000667.1:g.78845646A>G GRCh37
NC_000005.8:g.78881402A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948497.1:n.72+2179A>G
XR_948498.1:n.159+1986A>G
XR_948499.1:n.67+1521A>G
XR_948497.2:n.72+2179A>G
XR_948498.2:n.159+1986A>G
XR_948499.2:n.225+1521A>G