Canonical Allele Identifier: CA1796404045
Gene:

Linked Data

dbSNP Id: rs1810028914

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191086C>T , CM000670.2:g.79191086C>T GRCh38
NC_000008.10:g.80103321C>T , CM000670.1:g.80103321C>T GRCh37
NC_000008.9:g.80265876C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745720.1:n.105+715C>T