Canonical Allele Identifier: CA2206404210
Gene:

Linked Data

dbSNP Id: rs1898215846

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249553C>G , CM000678.2:g.9249553C>G GRCh38
NC_000016.9:g.9343410C>G , CM000678.1:g.9343410C>G GRCh37
NC_000016.8:g.9250911C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64820C>G