Canonical Allele Identifier: CA1065217487
Gene:

Linked Data

dbSNP Id: rs899877262

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597947T>A , CM000666.2:g.89597947T>A GRCh38
NC_000004.11:g.90519098T>A , CM000666.1:g.90519098T>A GRCh37
NC_000004.10:g.90738121T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+10007T>A
XR_938987.1:n.433-206T>A
XR_938988.1:n.299-206T>A
XR_938990.1:n.298+10007T>A
XR_938991.1:n.298+10007T>A
XR_938992.1:n.298+10007T>A
XR_938994.1:n.643+10007T>A
XR_938995.1:n.477+10007T>A
XR_938996.1:n.298+10007T>A
XR_938997.1:n.298+10007T>A
XR_938986.2:n.323+10007T>A
XR_938987.2:n.493-206T>A