Canonical Allele Identifier: CA134548283
Gene:

Linked Data

dbSNP Id: rs968914524

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169698A>G , CM000668.2:g.8169698A>G GRCh38
NC_000006.11:g.8169931A>G , CM000668.1:g.8169931A>G GRCh37
NC_000006.10:g.8114930A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.82+11438A>G
XR_926441.1:n.189+1778A>G
XR_926442.1:n.82+11438A>G
XR_926443.1:n.82+11438A>G
XR_001743950.1:n.179+1778A>G
XR_926440.2:n.74+11438A>G
XR_926441.2:n.179+1778A>G
XR_926443.2:n.83+11438A>G