Canonical Allele Identifier: CA1796404027
Gene:

Linked Data

dbSNP Id: rs1810028010

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191027T>C , CM000670.2:g.79191027T>C GRCh38
NC_000008.10:g.80103262T>C , CM000670.1:g.80103262T>C GRCh37
NC_000008.9:g.80265817T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+656T>C