Canonical Allele Identifier: CA2144473211
Gene:

Linked Data

dbSNP Id: rs1895390082

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807098C>G , CM000676.2:g.68807098C>G GRCh38
NC_000014.8:g.69273815C>G , CM000676.1:g.69273815C>G GRCh37
NC_000014.7:g.68343568C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-444G>C XP_011535743.1:n.673-444G>C
XM_011537442.1:c.673-444G>C XP_011535744.1:n.673-444G>C
XM_011537443.1:c.673-444G>C XP_011535745.1:n.673-444G>C