Canonical Allele Identifier: CA1889344555
Gene:

Linked Data

dbSNP Id: rs1832130742

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697643T>C , CM000672.2:g.8697643T>C GRCh38
NC_000010.10:g.8739606T>C , CM000672.1:g.8739606T>C GRCh37
NC_000010.9:g.8779612T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27842A>G