Canonical Allele Identifier: CA1800979765
Gene:

Linked Data

dbSNP Id: rs1808584503

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981112A>G , CM000670.2:g.88981112A>G GRCh38
NC_000008.10:g.89993341A>G , CM000670.1:g.89993341A>G GRCh37
NC_000008.9:g.90062457A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956667.1:n.179-99051T>C