Canonical Allele Identifier: CA1112378885
Gene:

Linked Data

dbSNP Id: rs1804275989
gnomAD v3: 8-31176665-A-C
gnomAD v4: 8-31176665-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176665A>C , CM000670.2:g.31176665A>C GRCh38
NC_000008.10:g.31034181A>C , CM000670.1:g.31034181A>C GRCh37
NC_000008.9:g.31153723A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949642.1:n.271-77A>C
XR_949643.1:n.87+27T>G
XR_949644.1:n.87+27T>G
XR_949645.1:n.87+27T>G
XR_949646.1:n.87+27T>G
XR_949647.1:n.700+27T>G
XR_949648.1:n.602+27T>G