Canonical Allele Identifier: CA776019737
Gene:

Linked Data

dbSNP Id: rs1475044075
gnomAD v3: 18-10321246-A-C
gnomAD v4: 18-10321246-A-C
MyVariant Identifiers: chr18:g.10321243A>C (hg19) chr18:g.10321246A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.10321246A>C , CM000680.2:g.10321246A>C GRCh38
NC_000018.9:g.10321243A>C , CM000680.1:g.10321243A>C GRCh37
NC_000018.8:g.10311243A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_935138.1:n.665+902T>G
XR_001753344.1:n.650+902T>G
XR_001753345.1:n.875T>G
XR_001753346.1:n.549+902T>G
Search 100 bp 5'
Search 100 bp 3'