Linked Data
ClinVar Variation Id:
2715314
ClinVar RCV Id:
RCV003518264
MyVariant Identifiers:
chr17:g.4855163C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4951868C>T , CM000679.2:g.4951868C>T | GRCh38 |
| NC_000017.10:g.4855163C>T , CM000679.1:g.4855163C>T | GRCh37 |
| NC_000017.9:g.4795908C>T | NCBI36 |
| NG_012063.2:g.10778C>T | |
| NG_032945.1:g.2219G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000519602.6:c.39C>T MANE Select | ENSP00000430055.2:p.Asp13= | |
| ENST00000323997.10:c.39C>T | ENSP00000324105.6:p.Asp13= | |
| ENST00000518175.1:c.39C>T | ENSP00000431087.1:p.Asp13= | |
| ENST00000518972.5:n.105C>T | ||
| ENST00000519266.5:c.39C>T | ENSP00000467270.1:p.Asp13= | |
| ENST00000519300.1:n.125C>T | ||
| ENST00000519584.5:c.39C>T | ENSP00000430636.1:p.Asp13= | |
| ENST00000519602.5:c.39C>T | ENSP00000430055.1:p.Asp13= | |
| ENST00000519834.5:n.105C>T | ||
| ENST00000520221.5:c.39C>T | ENSP00000467444.1:p.Asp13= | |
| ENST00000521659.5:c.39C>T | ENSP00000430554.1:p.Asp13= | |
| ENST00000521811.5:c.39C>T | ENSP00000464874.1:p.Asp13= | |
| ENST00000522249.5:c.39C>T | ENSP00000428811.1:p.Asp13= | |
| ENST00000522301.5:c.39C>T | ENSP00000465697.1:p.Asp13= | |
| ENST00000522798.5:c.39C>T | ENSP00000428502.1:p.Asp13= | |
| ENST00000571235.5:n.105C>T | ||
| NM_001193503.1:c.39C>T | NP_001180432.1:p.Asp13= | |
| NM_001976.4:c.39C>T | NP_001967.3:p.Asp13= | |
| NM_053013.3:c.39C>T | NP_443739.3:p.Asp13= | |
| XM_005256521.2:c.66C>T | XP_005256578.1:p.Asp22= | |
| XM_011523729.1:c.39C>T | XP_011522031.1:p.Asp13= | |
| XM_017024346.2:c.39C>T | XP_016879835.1:p.Asp13= | |
| NM_001193503.2:c.39C>T | NP_001180432.1:p.Asp13= | |
| NM_001374523.1:c.39C>T | NP_001361452.1:p.Asp13= | |
| NM_001374524.1:c.66C>T | NP_001361453.1:p.Asp22= | |
| NM_001976.5:c.39C>T | NP_001967.3:p.Asp13= | |
| NM_053013.4:c.39C>T MANE Select | NP_443739.3:p.Asp13= |