Canonical Allele Identifier: CA2136398867
Gene:

Linked Data

dbSNP Id: rs1595986771

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856902A>C , CM000676.2:g.50856902A>C GRCh38
NC_000014.8:g.51323620A>C , CM000676.1:g.51323620A>C GRCh37
NC_000014.7:g.50393370A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1196T>G
XR_943848.2:n.643+1196T>G