Canonical Allele Identifier: CA702501661
Gene:

Linked Data

dbSNP Id: rs1203037224

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853078T>C , CM000675.2:g.94853078T>C GRCh38
NC_000013.10:g.95505332T>C , CM000675.1:g.95505332T>C GRCh37
NC_000013.9:g.94303333T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52386T>C