Canonical Allele Identifier: CA2762576396
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655969T>C , CM000666.2:g.89655969T>C GRCh38
NC_000004.11:g.90577120T>C , CM000666.1:g.90577120T>C GRCh37
NC_000004.10:g.90796143T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28052T>C
XR_938987.1:n.688+28052T>C
XR_938988.1:n.554+28052T>C
XR_938990.1:n.299-35316T>C
XR_938991.1:n.434+28052T>C
XR_938994.1:n.779+28052T>C
XR_938995.1:n.613+28052T>C
XR_938986.2:n.459+28052T>C
XR_938987.2:n.748+28052T>C