Linked Data
ClinVar Variation Id:
1608324
ClinVar RCV Id:
RCV002162891
dbSNP Id:
rs2104285371
MyVariant Identifiers:
chr2:g.96919849C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96254111C>A , CM000664.2:g.96254111C>A | GRCh38 |
| NC_000002.11:g.96919849C>A , CM000664.1:g.96919849C>A | GRCh37 |
| NC_000002.10:g.96283576C>A | NCBI36 |
| NG_027695.1:g.16903G>T , LRG_528:g.16903G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258439.8:c.414G>T MANE Select | ENSP00000258439.3:p.Leu138= | |
| ENST00000258439.7:c.414G>T | ENSP00000258439.2:p.Leu138= | |
| ENST00000432959.1:c.414G>T | ENSP00000416660.1:p.Leu138= | |
| ENST00000435268.1:c.162G>T | ENSP00000411810.1:p.Leu54= | |
| NM_001193304.2:c.414G>T | NP_001180233.1:p.Leu138= | |
| NM_017849.3:c.414G>T , LRG_528t1:c.414G>T | NP_060319.1:p.Leu138= | |
| XM_017004450.1:c.-505G>T | XP_016859939.1:n.-505G>T | |
| XM_017004452.1:c.162G>T | XP_016859941.1:p.Leu54= | |
| NM_001193304.3:c.414G>T | NP_001180233.1:p.Leu138= | |
| NM_017849.4:c.414G>T MANE Select | NP_060319.1:p.Leu138= |