Canonical Allele Identifier: CA207989729
Gene:

Linked Data

dbSNP Id: rs1032082056

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812874T>C , CM000672.2:g.57812874T>C GRCh38
NC_000010.10:g.59572634T>C , CM000672.1:g.59572634T>C GRCh37
NC_000010.9:g.59242640T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34418A>G
XR_001747454.1:n.85+34418A>G