Linked Data
ClinVar Variation Id:
337068
dbSNP Id:
rs886056328
gnomAD v2:
2-74588704-C-T
gnomAD v3:
2-74361577-C-T
gnomAD v4:
2-74361577-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.74361577C>T , CM000664.2:g.74361577C>T | GRCh38 |
| NC_000002.11:g.74588704C>T , CM000664.1:g.74588704C>T | GRCh37 |
| NC_000002.10:g.74442212C>T | NCBI36 |
| NG_008735.2:g.35511G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361874.8:c.3744G>A | ENSP00000354791.4:p.Ala1248= | |
| ENST00000628224.3:c.3759G>A MANE Select | ENSP00000487279.2:p.Ala1253= | |
| ENST00000680606.1:c.3708G>A | ENSP00000505612.1:p.Ala1236= | |
| ENST00000361874.7:c.3759G>A | ENSP00000354791.3:p.Ala1253= | |
| ENST00000394003.7:c.3738G>A | ENSP00000377571.3:p.Ala1246= | |
| ENST00000409240.5:c.3633G>A | ENSP00000386406.1:p.Ala1211= | |
| ENST00000409438.5:c.3342G>A | ENSP00000387270.1:p.Ala1114= | |
| ENST00000409567.7:c.3684G>A | ENSP00000386843.3:p.Ala1228= | |
| ENST00000409868.5:c.3693G>A | ENSP00000387327.1:p.Ala1231= | |
| ENST00000434055.5:c.*1043G>A | ENSP00000416711.1:n.*1043G>A | |
| ENST00000451608.2:c.498G>A | ENSP00000416453.2:p.Ala166= | |
| ENST00000466110.5:n.4996G>A | ||
| ENST00000491465.5:n.2022G>A | ||
| ENST00000497666.1:n.97-40G>A | ||
| ENST00000628224.2:c.3693G>A | ENSP00000487279.1:p.Ala1231= | |
| ENST00000633691.1:c.3357G>A | ENSP00000487724.1:p.Ala1119= | |
| NM_001135040.2:c.3684G>A | NP_001128512.1:p.Ala1228= | |
| NM_001135041.2:c.3342G>A | NP_001128513.1:p.Ala1114= | |
| NM_001190836.1:c.3633G>A | NP_001177765.1:p.Ala1211= | |
| NM_001190837.1:c.3738G>A | NP_001177766.1:p.Ala1246= | |
| NM_004082.4:c.3759G>A | NP_004073.2:p.Ala1253= | |
| NM_023019.3:c.3357G>A | NP_075408.1:p.Ala1119= | |
| NR_033935.1:n.4028G>A | ||
| NM_001135040.3:c.3684G>A | NP_001128512.1:p.Ala1228= | |
| NM_001135041.3:c.3342G>A | NP_001128513.1:p.Ala1114= | |
| NM_001190836.2:c.3633G>A | NP_001177765.1:p.Ala1211= | |
| NM_001190837.2:c.3738G>A | NP_001177766.1:p.Ala1246= | |
| NM_001378991.1:c.3708G>A | NP_001365920.1:p.Ala1236= | |
| NM_001378992.1:c.3690G>A | NP_001365921.1:p.Ala1230= | |
| NM_004082.5:c.3759G>A MANE Select | NP_004073.2:p.Ala1253= | |
| NM_023019.4:c.3357G>A | NP_075408.1:p.Ala1119= | |
| NR_033935.2:n.3807G>A |