Linked Data
ClinVar Variation Id:
2805690
ClinVar RCV Id:
RCV003762402
MyVariant Identifiers:
chr2:g.203420698G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202555975G>A , CM000664.2:g.202555975G>A | GRCh38 |
| NC_000002.11:g.203420698G>A , CM000664.1:g.203420698G>A | GRCh37 |
| NC_000002.10:g.203128943G>A | NCBI36 |
| NG_009363.1:g.184649G>A , LRG_712:g.184649G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.2310G>A MANE Select | ENSP00000363708.4:p.Arg770= | |
| ENST00000638587.1:c.2241G>A | ENSP00000491062.1:n.2241G>A | |
| ENST00000374574.2:c.1586+3087G>A | ENSP00000363702.2:n.1586+3087G>A | |
| ENST00000374580.8:c.2310G>A | ENSP00000363708.4:p.Arg770= | |
| NM_001204.6:c.2310G>A , LRG_712t1:c.2310G>A | NP_001195.2:p.Arg770= | |
| XM_011511687.1:c.2310G>A | XP_011509989.1:p.Arg770= | |
| XM_011511688.1:c.1586+3087G>A | XP_011509990.1:n.1586+3087G>A | |
| NM_001204.7:c.2310G>A MANE Select | NP_001195.2:p.Arg770= |