Linked Data
ClinVar Variation Id:
2133093
ClinVar RCV Id:
RCV003056206
gnomAD v4:
18-79679989-C-T
MyVariant Identifiers:
chr18:g.77439989C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.79679989C>T , CM000680.2:g.79679989C>T | GRCh38 |
| NC_000018.9:g.77439989C>T , CM000680.1:g.77439989C>T | GRCh37 |
| NC_000018.8:g.75540977C>T | NCBI36 |
| NG_007988.1:g.5189C>T , LRG_236:g.5189C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000613122.5:c.42C>T MANE Select | ENSP00000484525.2:p.Ala14= | |
| ENST00000075430.11:c.42C>T | ENSP00000075430.7:p.Ala14= | |
| ENST00000613122.4:c.42C>T | ENSP00000484525.1:p.Ala14= | |
| NM_004715.4:c.42C>T , LRG_236t1:c.42C>T | NP_004706.3:p.Ala14= | |
| NM_048368.3:c.42C>T | NP_430255.2:p.Ala14= | |
| XM_005266782.2:c.42C>T | XP_005266839.1:p.Ala14= | |
| XM_011526261.1:c.42C>T | XP_011524563.1:p.Ala14= | |
| NM_001318511.1:c.42C>T | NP_001305440.1:p.Ala14= | |
| NM_001318511.2:c.42C>T | NP_001305440.1:p.Ala14= | |
| NM_004715.5:c.42C>T MANE Select | NP_004706.3:p.Ala14= | |
| NM_048368.4:c.42C>T | NP_430255.2:p.Ala14= |