Canonical Allele Identifier: CA1889258898
Gene:

Linked Data

dbSNP Id: rs1832545090

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8563970T>C , CM000672.2:g.8563970T>C GRCh38
NC_000010.10:g.8605933T>C , CM000672.1:g.8605933T>C GRCh37
NC_000010.9:g.8645939T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930640.1:n.73-25318T>C