Canonical Allele Identifier: CA1608914068
Gene:

Linked Data

dbSNP Id: rs1759196449

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169833T>G , CM000668.2:g.8169833T>G GRCh38
NC_000006.11:g.8170066T>G , CM000668.1:g.8170066T>G GRCh37
NC_000006.10:g.8115065T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11573T>G
XR_926441.1:n.189+1913T>G
XR_926442.1:n.82+11573T>G
XR_926443.1:n.82+11573T>G
XR_001743950.1:n.179+1913T>G
XR_926440.2:n.74+11573T>G
XR_926441.2:n.179+1913T>G
XR_926443.2:n.83+11573T>G