Canonical Allele Identifier: CA1889344517
Gene:

Linked Data

dbSNP Id: rs1588445899

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697563A>C , CM000672.2:g.8697563A>C GRCh38
NC_000010.10:g.8739526A>C , CM000672.1:g.8739526A>C GRCh37
NC_000010.9:g.8779532A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930641.1:n.33-27762T>G