Canonical Allele Identifier: CA1475277621
Gene:

Linked Data

dbSNP Id: rs1721484483

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89597861T>C , CM000666.2:g.89597861T>C GRCh38
NC_000004.11:g.90519012T>C , CM000666.1:g.90519012T>C GRCh37
NC_000004.10:g.90738035T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.298+9921T>C
XR_938987.1:n.433-292T>C
XR_938988.1:n.299-292T>C
XR_938990.1:n.298+9921T>C
XR_938991.1:n.298+9921T>C
XR_938992.1:n.298+9921T>C
XR_938994.1:n.643+9921T>C
XR_938995.1:n.477+9921T>C
XR_938996.1:n.298+9921T>C
XR_938997.1:n.298+9921T>C
XR_938986.2:n.323+9921T>C
XR_938987.2:n.493-292T>C