Canonical Allele Identifier: CA1475277651
Gene:

Linked Data

dbSNP Id: rs1721486210

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597921dup , CM000666.2:g.89597921dup GRCh38
NC_000004.11:g.90519072dup , CM000666.1:g.90519072dup GRCh37
NC_000004.10:g.90738095dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9981dup
XR_938987.1:n.433-232dup
XR_938988.1:n.299-232dup
XR_938990.1:n.298+9981dup
XR_938991.1:n.298+9981dup
XR_938992.1:n.298+9981dup
XR_938994.1:n.643+9981dup
XR_938995.1:n.477+9981dup
XR_938996.1:n.298+9981dup
XR_938997.1:n.298+9981dup
XR_938986.2:n.323+9981dup
XR_938987.2:n.493-232dup