Canonical Allele Identifier: CA2255111918
Gene:

Linked Data

dbSNP Id: rs1597650325

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237240T>C , CM000679.2:g.30237240T>C GRCh38
NC_000017.10:g.28564258T>C , CM000679.1:g.28564258T>C GRCh37
NC_000017.9:g.25588384T>C NCBI36
NG_011747.2:g.3697A>G

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+170T>C
XR_001752824.1:n.280+170T>C