Canonical Allele Identifier: CA2791024201
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812518A>G , CM000673.2:g.34812518A>G GRCh38
NC_000011.9:g.34834065A>G , CM000673.1:g.34834065A>G GRCh37
NC_000011.8:g.34790641A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57911A>G
XR_931188.1:n.693+57911A>G
XR_931189.1:n.854+57911A>G
XR_931190.1:n.639+57911A>G
XR_931191.1:n.689+57911A>G
XR_001748174.1:n.855+57911A>G
XR_001748176.1:n.1016+57911A>G
XR_002957246.1:n.639+57911A>G