Canonical Allele Identifier: CA2112050496
Gene:

Linked Data

dbSNP Id: rs1878598828

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94852998T>G , CM000675.2:g.94852998T>G GRCh38
NC_000013.10:g.95505252T>G , CM000675.1:g.95505252T>G GRCh37
NC_000013.9:g.94303253T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52466T>G