Canonical Allele Identifier: CA262840972
Gene:

Linked Data

dbSNP Id: rs556500039

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807204G>A , CM000676.2:g.68807204G>A GRCh38
NC_000014.8:g.69273921G>A , CM000676.1:g.69273921G>A GRCh37
NC_000014.7:g.68343674G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-550C>T XP_011535743.1:n.673-550C>T
XM_011537442.1:c.673-550C>T XP_011535744.1:n.673-550C>T
XM_011537443.1:c.673-550C>T XP_011535745.1:n.673-550C>T