Canonical Allele Identifier: CA721980873
Gene:

Linked Data

dbSNP Id: rs1158922880

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.56610658A>G , CM000678.2:g.56610658A>G GRCh38
NC_000016.9:g.56644570A>G , CM000678.1:g.56644570A>G GRCh37
NC_000016.8:g.55202071A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933616.1:n.605+658T>C