Canonical Allele Identifier: CA170720
Gene:

Linked Data

ClinVar Variation Id: 155878
ClinVar RCV Id: RCV000143995
dbSNP Id: rs9397435

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151630085A>G , CM000668.2:g.151630085A>G GRCh38
NC_000006.11:g.151951220A>G , CM000668.1:g.151951220A>G GRCh37
NC_000006.10:g.151992913A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943113.1:n.2496+103A>G
XR_943115.1:n.2496+103A>G