Canonical Allele Identifier: CA260835602
Gene:

Linked Data

dbSNP Id: rs946828093

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857027T>G , CM000676.2:g.50857027T>G GRCh38
NC_000014.8:g.51323745T>G , CM000676.1:g.51323745T>G GRCh37
NC_000014.7:g.50393495T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1071A>C
XR_943848.2:n.643+1071A>C