Canonical Allele Identifier: CA964316780
Gene:

Linked Data

dbSNP Id: rs112347546

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807207G>C , CM000676.2:g.68807207G>C GRCh38
NC_000014.8:g.69273924G>C , CM000676.1:g.69273924G>C GRCh37
NC_000014.7:g.68343677G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-553C>G XP_011535743.1:n.673-553C>G
XM_011537442.1:c.673-553C>G XP_011535744.1:n.673-553C>G
XM_011537443.1:c.673-553C>G XP_011535745.1:n.673-553C>G