Canonical Allele Identifier: CA2717766959
Gene:

Linked Data

dbSNP Id: rs1401139131

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88981334A>C , CM000670.2:g.88981334A>C GRCh38
NC_000008.10:g.89993563A>C , CM000670.1:g.89993563A>C GRCh37
NC_000008.9:g.90062679A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956667.1:n.179-99273T>G