Canonical Allele Identifier: CA1475305060
Gene:

Linked Data

dbSNP Id: rs1722651539

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655947T>C , CM000666.2:g.89655947T>C GRCh38
NC_000004.11:g.90577098T>C , CM000666.1:g.90577098T>C GRCh37
NC_000004.10:g.90796121T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28030T>C
XR_938987.1:n.688+28030T>C
XR_938988.1:n.554+28030T>C
XR_938990.1:n.299-35338T>C
XR_938991.1:n.434+28030T>C
XR_938994.1:n.779+28030T>C
XR_938995.1:n.613+28030T>C
XR_938986.2:n.459+28030T>C
XR_938987.2:n.748+28030T>C