Canonical Allele Identifier: CA2298481222
Gene:

Linked Data

dbSNP Id: rs907485337

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.41477648A>C , CM000680.2:g.41477648A>C GRCh38
NC_000018.9:g.39057612A>C , CM000680.1:g.39057612A>C GRCh37
NC_000018.8:g.37311610A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935409.1:n.86-26486A>C