Canonical Allele Identifier: CA613876325
Gene:

Linked Data

dbSNP Id: rs1485910033

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50857041A>G , CM000676.2:g.50857041A>G GRCh38
NC_000014.8:g.51323759A>G , CM000676.1:g.51323759A>G GRCh37
NC_000014.7:g.50393509A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943848.1:n.282+1057T>C
XR_943848.2:n.643+1057T>C