Canonical Allele Identifier: CA1769199589
Gene:

Linked Data

dbSNP Id: rs11204093

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130235G>C , CM000670.2:g.20130235G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+316G>C
XR_949563.2:n.3400+316G>C