Canonical Allele Identifier: CA1912720940
Gene:

Linked Data

dbSNP Id: rs1839462291

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812938C>G , CM000672.2:g.57812938C>G GRCh38
NC_000010.10:g.59572698C>G , CM000672.1:g.59572698C>G GRCh37
NC_000010.9:g.59242704C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34354G>C
XR_001747454.1:n.85+34354G>C