Canonical Allele Identifier: CA2136398948
Gene:

Linked Data

dbSNP Id: rs2045894332

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857076G>T , CM000676.2:g.50857076G>T GRCh38
NC_000014.8:g.51323794G>T , CM000676.1:g.51323794G>T GRCh37
NC_000014.7:g.50393544G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1022C>A
XR_943848.2:n.643+1022C>A