Canonical Allele Identifier: CA2144473257
Gene:

Linked Data

dbSNP Id: rs1895391354

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807196G>A , CM000676.2:g.68807196G>A GRCh38
NC_000014.8:g.69273913G>A , CM000676.1:g.69273913G>A GRCh37
NC_000014.7:g.68343666G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-542C>T XP_011535743.1:n.673-542C>T
XM_011537442.1:c.673-542C>T XP_011535744.1:n.673-542C>T
XM_011537443.1:c.673-542C>T XP_011535745.1:n.673-542C>T