Canonical Allele Identifier: CA613876317
Gene:

Linked Data

dbSNP Id: rs1290834828

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50856889G>T , CM000676.2:g.50856889G>T GRCh38
NC_000014.8:g.51323607G>T , CM000676.1:g.51323607G>T GRCh37
NC_000014.7:g.50393357G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943848.1:n.282+1209C>A
XR_943848.2:n.643+1209C>A