Canonical Allele Identifier: CA855697442
Gene:

Linked Data

dbSNP Id: rs1188404779

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.79191029C>T , CM000670.2:g.79191029C>T GRCh38
NC_000008.10:g.80103264C>T , CM000670.1:g.80103264C>T GRCh37
NC_000008.9:g.80265819C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745720.1:n.105+658C>T