Canonical Allele Identifier: CA1886690307
Gene:

Linked Data

dbSNP Id: rs1831781666

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3366839T>C , CM000672.2:g.3366839T>C GRCh38
NC_000010.10:g.3409031T>C , CM000672.1:g.3409031T>C GRCh37
NC_000010.9:g.3399031T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131187.1:n.162+47983T>C