Canonical Allele Identifier: CA1085755587
Gene:

Linked Data

dbSNP Id: rs1279031689
gnomAD v3: 6-8228603-T-C
gnomAD v4: 6-8228603-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8228603T>C , CM000668.2:g.8228603T>C GRCh38
NC_000006.11:g.8228836T>C , CM000668.1:g.8228836T>C GRCh37
NC_000006.10:g.8173835T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926440.1:n.83-1511T>C
XR_926441.1:n.190-10328T>C
XR_926442.1:n.83-1511T>C
XR_926443.1:n.83-10328T>C
XR_001743950.1:n.180-10328T>C
XR_926440.2:n.75-1511T>C
XR_926441.2:n.180-10328T>C
XR_926443.2:n.84-10328T>C