Linked Data
ClinVar Variation Id:
2701314
ClinVar RCV Id:
RCV003536252
gnomAD v4:
7-21880800-C-T
MyVariant Identifiers:
chr7:g.21920418C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21880800C>T , CM000669.2:g.21880800C>T | GRCh38 |
| NC_000007.13:g.21920418C>T , CM000669.1:g.21920418C>T | GRCh37 |
| NC_000007.12:g.21886943C>T | NCBI36 |
| NG_012886.2:g.342586C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.12294C>T MANE Select | ENSP00000475939.1:p.Gly4098= | |
| ENST00000328843.10:c.12315C>T | ENSP00000330671.7:p.Gly4105= | |
| ENST00000409508.7:c.12294C>T | ENSP00000475939.1:p.Gly4098= | |
| ENST00000620169.4:c.12315C>T | ENSP00000481693.1:p.Gly4105= | |
| NM_001277115.1:c.12294C>T | NP_001264044.1:p.Gly4098= | |
| NM_001277115.2:c.12294C>T MANE Select | NP_001264044.1:p.Gly4098= |