Canonical Allele Identifier: CA2206404142
Gene:

Linked Data

dbSNP Id: rs1898214438

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249441T>C , CM000678.2:g.9249441T>C GRCh38
NC_000016.9:g.9343298T>C , CM000678.1:g.9343298T>C GRCh37
NC_000016.8:g.9250799T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64708T>C