Canonical Allele Identifier: CA1105646075
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032370466
gnomAD v3: 7-107920024-T-C
gnomAD v4: 7-107920024-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920024T>C , CM000669.2:g.107920024T>C GRCh38
NC_000007.13:g.107560469T>C , CM000669.1:g.107560469T>C GRCh37
NC_000007.12:g.107347705T>C NCBI36
NG_008045.1:g.33884T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*765T>C MANE Select ENSP00000205402.3:n.*765T>C
ENST00000205402.9:c.*765T>C ENSP00000205402.3:n.*765T>C
ENST00000417551.5:c.*124+641T>C ENSP00000390667.1:n.*124+641T>C
NM_000108.4:c.*765T>C NP_000099.2:n.*765T>C
NM_001289750.1:c.*765T>C NP_001276679.1:n.*765T>C
NM_001289751.1:c.*765T>C NP_001276680.1:n.*765T>C
NM_001289752.1:c.*765T>C NP_001276681.1:n.*765T>C
NM_000108.5:c.*765T>C MANE Select NP_000099.2:n.*765T>C
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