Canonical Allele Identifier: CA1912720771
Gene:

Linked Data

dbSNP Id: rs1839459739

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812606A>T , CM000672.2:g.57812606A>T GRCh38
NC_000010.10:g.59572366A>T , CM000672.1:g.59572366A>T GRCh37
NC_000010.9:g.59242372A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945979.1:n.68+34686T>A
XR_001747454.1:n.85+34686T>A