Canonical Allele Identifier: CA565403886
Gene:

Linked Data

dbSNP Id: rs1307761428
gnomAD v2: 6-8169757-T-G
gnomAD v3: 6-8169524-T-G
gnomAD v4: 6-8169524-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.8169524T>G , CM000668.2:g.8169524T>G GRCh38
NC_000006.11:g.8169757T>G , CM000668.1:g.8169757T>G GRCh37
NC_000006.10:g.8114756T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926440.1:n.82+11264T>G
XR_926441.1:n.189+1604T>G
XR_926442.1:n.82+11264T>G
XR_926443.1:n.82+11264T>G
XR_001743950.1:n.179+1604T>G
XR_926440.2:n.74+11264T>G
XR_926441.2:n.179+1604T>G
XR_926443.2:n.83+11264T>G