Canonical Allele Identifier: CA964316715
Gene:

Linked Data

dbSNP Id: rs1895390202

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807103A>G , CM000676.2:g.68807103A>G GRCh38
NC_000014.8:g.69273820A>G , CM000676.1:g.69273820A>G GRCh37
NC_000014.7:g.68343573A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537441.1:c.673-449T>C XP_011535743.1:n.673-449T>C
XM_011537442.1:c.673-449T>C XP_011535744.1:n.673-449T>C
XM_011537443.1:c.673-449T>C XP_011535745.1:n.673-449T>C