Linked Data
ClinVar Variation Id:
2656473
ClinVar RCV Id:
RCV003431801
MyVariant Identifiers:
chr6:g.32634301T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32666524T>G , CM000668.2:g.32666524T>G | GRCh38 |
| NC_000006.11:g.32634301T>G , CM000668.1:g.32634301T>G | GRCh37 |
| NC_000006.10:g.32742279T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000434651.7:c.84A>C MANE Select | ENSP00000407332.2:p.Leu28= | |
| ENST00000374943.8:c.84A>C | ENSP00000364080.4:p.Leu28= | |
| ENST00000399079.7:c.84A>C | ENSP00000382029.3:p.Leu28= | |
| ENST00000399082.7:c.84A>C | ENSP00000382032.3:p.Leu28= | |
| ENST00000399084.5:c.84A>C | ENSP00000382034.1:p.Leu28= | |
| ENST00000434651.6:c.84A>C | ENSP00000407332.2:p.Leu28= | |
| ENST00000484729.2:c.84A>C | ENSP00000436686.1:p.Leu28= | |
| ENST00000487676.1:n.115A>C | ||
| NM_001243961.1:c.84A>C | NP_001230890.1:p.Leu28= | |
| NM_002123.4:c.84A>C | NP_002114.3:p.Leu28= | |
| NM_001243961.2:c.84A>C | NP_001230890.1:p.Leu28= | |
| NM_002123.5:c.84A>C MANE Select | NP_002114.3:p.Leu28= |