Linked Data
ClinVar Variation Id:
2924270
ClinVar RCV Id:
RCV003786020
MyVariant Identifiers:
chr10:g.121429479C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119669967C>T , CM000672.2:g.119669967C>T | GRCh38 |
| NC_000010.10:g.121429479C>T , CM000672.1:g.121429479C>T | GRCh37 |
| NC_000010.9:g.121419469C>T | NCBI36 |
| NG_016125.1:g.23598C>T , LRG_742:g.23598C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.297C>T MANE Select | ENSP00000358081.4:p.Leu99= | |
| ENST00000369085.7:c.297C>T | ENSP00000358081.3:p.Leu99= | |
| ENST00000450186.1:c.123C>T | ENSP00000410036.1:p.Leu41= | |
| NM_004281.3:c.297C>T , LRG_742t1:c.297C>T | NP_004272.2:p.Leu99= | |
| XM_005270287.1:c.297C>T | XP_005270344.1:p.Leu99= | |
| XM_005270287.2:c.297C>T | XP_005270344.1:p.Leu99= | |
| NM_004281.4:c.297C>T MANE Select | NP_004272.2:p.Leu99= |