Canonical Allele Identifier: CA101489349
Gene:

Linked Data

dbSNP Id: rs534009821

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89655820C>T , CM000666.2:g.89655820C>T GRCh38
NC_000004.11:g.90576971C>T , CM000666.1:g.90576971C>T GRCh37
NC_000004.10:g.90795994C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938986.1:n.434+27903C>T
XR_938987.1:n.688+27903C>T
XR_938988.1:n.554+27903C>T
XR_938990.1:n.299-35465C>T
XR_938991.1:n.434+27903C>T
XR_938994.1:n.779+27903C>T
XR_938995.1:n.613+27903C>T
XR_938986.2:n.459+27903C>T
XR_938987.2:n.748+27903C>T