Canonical Allele Identifier: CA220638173
Gene:

Linked Data

dbSNP Id: rs749228613

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34759459A>T , CM000673.2:g.34759459A>T GRCh38
NC_000011.9:g.34781006A>T , CM000673.1:g.34781006A>T GRCh37
NC_000011.8:g.34737582A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+4852A>T
XR_931188.1:n.693+4852A>T
XR_931189.1:n.854+4852A>T
XR_931190.1:n.639+4852A>T
XR_931191.1:n.689+4852A>T
XR_001748174.1:n.855+4852A>T
XR_001748176.1:n.1016+4852A>T
XR_002957246.1:n.639+4852A>T