Canonical Allele Identifier: CA2144473225
Gene:

Linked Data

dbSNP Id: rs1895390432

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807133T>C , CM000676.2:g.68807133T>C GRCh38
NC_000014.8:g.69273850T>C , CM000676.1:g.69273850T>C GRCh37
NC_000014.7:g.68343603T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537441.1:c.673-479A>G XP_011535743.1:n.673-479A>G
XM_011537442.1:c.673-479A>G XP_011535744.1:n.673-479A>G
XM_011537443.1:c.673-479A>G XP_011535745.1:n.673-479A>G