Canonical Allele Identifier: CA206723627
Gene:

Linked Data

dbSNP Id: rs372907625

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318692C>T , CM000672.2:g.43318692C>T GRCh38
NC_000010.10:g.43814140C>T , CM000672.1:g.43814140C>T GRCh37
NC_000010.9:g.43134146C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+97C>T
XR_945902.2:n.198+97C>T