Canonical Allele Identifier: CA1796404103
Gene:

Linked Data

dbSNP Id: rs1586313863

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191210A>C , CM000670.2:g.79191210A>C GRCh38
NC_000008.10:g.80103445A>C , CM000670.1:g.80103445A>C GRCh37
NC_000008.9:g.80266000A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+839A>C