Canonical Allele Identifier: CA666858106
Gene:

Linked Data

dbSNP Id: rs1213207411

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812988T>C , CM000672.2:g.57812988T>C GRCh38
NC_000010.10:g.59572748T>C , CM000672.1:g.59572748T>C GRCh37
NC_000010.9:g.59242754T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34304A>G
XR_001747454.1:n.85+34304A>G