Canonical Allele Identifier: CA101489373
Gene:

Linked Data

dbSNP Id: rs891330140

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89656004_89656010del , CM000666.2:g.89656004_89656010del GRCh38
NC_000004.11:g.90577155_90577161del , CM000666.1:g.90577155_90577161del GRCh37
NC_000004.10:g.90796178_90796184del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+28087_434+28093del
XR_938987.1:n.688+28087_688+28093del
XR_938988.1:n.554+28087_554+28093del
XR_938990.1:n.299-35281_299-35275del
XR_938991.1:n.434+28087_434+28093del
XR_938994.1:n.779+28087_779+28093del
XR_938995.1:n.613+28087_613+28093del
XR_938986.2:n.459+28087_459+28093del
XR_938987.2:n.748+28087_748+28093del