Canonical Allele Identifier: CA2144473255
Gene:

Linked Data

dbSNP Id: rs1457552192

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807195T>G , CM000676.2:g.68807195T>G GRCh38
NC_000014.8:g.69273912T>G , CM000676.1:g.69273912T>G GRCh37
NC_000014.7:g.68343665T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-541A>C XP_011535743.1:n.673-541A>C
XM_011537442.1:c.673-541A>C XP_011535744.1:n.673-541A>C
XM_011537443.1:c.673-541A>C XP_011535745.1:n.673-541A>C