Canonical Allele Identifier: CA14543049
Gene: CTDP1-DT HGNC NCBI

Linked Data

ClinVar Variation Id: 1242329
ClinVar RCV Id: RCV001648179
dbSNP Id: rs56246515
gnomAD v2: 18-77439756-G-A
gnomAD v3: 18-79679756-G-A
gnomAD v4: 18-79679756-G-A
MyVariant Identifiers: chr18:g.77439756G>A (hg19) chr18:g.79679756G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.79679756G>A , CM000680.2:g.79679756G>A GRCh38
NC_000018.9:g.77439756G>A , CM000680.1:g.77439756G>A GRCh37
NC_000018.8:g.75540744G>A NCBI36
NG_007988.1:g.4956G>A , LRG_236:g.4956G>A

Transcript Alleles

HGVS Amino-acid Change
XR_935692.1:n.20C>T
Search 100 bp 5'
Search 100 bp 3'