Canonical Allele Identifier: CA1608913916
Gene:

Linked Data

dbSNP Id: rs1759194361

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169695G>C , CM000668.2:g.8169695G>C GRCh38
NC_000006.11:g.8169928G>C , CM000668.1:g.8169928G>C GRCh37
NC_000006.10:g.8114927G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11435G>C
XR_926441.1:n.189+1775G>C
XR_926442.1:n.82+11435G>C
XR_926443.1:n.82+11435G>C
XR_001743950.1:n.179+1775G>C
XR_926440.2:n.74+11435G>C
XR_926441.2:n.179+1775G>C
XR_926443.2:n.83+11435G>C