Linked Data
ClinVar Variation Id:
434095
dbSNP Id:
rs147299402
ExAC:
20:49508634 C / A
gnomAD v2:
20-49508634-C-A
gnomAD v3:
20-50892097-C-A
gnomAD v4:
20-50892097-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.50892097C>A , CM000682.2:g.50892097C>A | GRCh38 |
| NC_000020.10:g.49508634C>A , CM000682.1:g.49508634C>A | GRCh37 |
| NC_000020.9:g.48942041C>A | NCBI36 |
| NG_034200.1:g.43894G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349014.8:c.2617G>T | ENSP00000342905.3:p.Asp873Tyr | |
| ENST00000371602.9:c.2617G>T | ENSP00000360662.2:p.Asp873Tyr | |
| ENST00000396029.8:c.2617G>T | ENSP00000379346.3:p.Asp873Tyr | |
| ENST00000396032.8:c.2617G>T | ENSP00000379349.2:p.Asp873Tyr | |
| ENST00000621696.5:c.2617G>T MANE Select | ENSP00000483881.1:p.Asp873Tyr | |
| ENST00000644386.1:c.202-2140G>T | ENSP00000493755.1:n.202-2140G>T | |
| ENST00000645081.1:c.1933G>T | ENSP00000495540.1:p.Asp645Tyr | |
| ENST00000673732.1:c.2833G>T | ENSP00000501294.1:p.Asp945Tyr | |
| ENST00000349014.7:c.2617G>T | ENSP00000342905.3:p.Asp873Tyr | |
| ENST00000371602.8:c.2617G>T | ENSP00000360662.2:p.Asp873Tyr | |
| ENST00000396029.7:c.2617G>T | ENSP00000379346.3:p.Asp873Tyr | |
| ENST00000396032.7:c.2617G>T | ENSP00000379349.2:p.Asp873Tyr | |
| ENST00000621696.4:c.2617G>T | ENSP00000483881.1:p.Asp873Tyr | |
| NM_001282531.1:c.2617G>T | NP_001269460.1:p.Asp873Tyr | |
| NM_001282532.1:c.2617G>T | NP_001269461.1:p.Asp873Tyr | |
| NM_015339.3:c.2617G>T | NP_056154.1:p.Asp873Tyr | |
| NM_181442.2:c.2617G>T | NP_852107.1:p.Asp873Tyr | |
| XM_011528747.1:c.2617G>T | XP_011527049.1:p.Asp873Tyr | |
| XM_011528748.1:c.2644G>T | XP_011527050.1:p.Asp882Tyr | |
| NM_001282531.2:c.2617G>T | NP_001269460.1:p.Asp873Tyr | |
| NM_001347511.1:c.2617G>T | NP_001334440.1:p.Asp873Tyr | |
| NM_015339.4:c.2617G>T | NP_056154.1:p.Asp873Tyr | |
| NM_181442.3:c.2617G>T | NP_852107.1:p.Asp873Tyr | |
| XM_011528747.2:c.2617G>T | XP_011527049.1:p.Asp873Tyr | |
| XM_011528748.2:c.2644G>T | XP_011527050.1:p.Asp882Tyr | |
| XM_017027758.1:c.2617G>T | XP_016883247.1:p.Asp873Tyr | |
| XM_017027759.1:c.2617G>T | XP_016883248.1:p.Asp873Tyr | |
| NM_001282531.3:c.2617G>T MANE Select | NP_001269460.1:p.Asp873Tyr | |
| NM_001347511.2:c.2617G>T | NP_001334440.1:p.Asp873Tyr | |
| NM_015339.5:c.2617G>T | NP_056154.1:p.Asp873Tyr | |
| NM_181442.4:c.2617G>T | NP_852107.1:p.Asp873Tyr | |
| NM_001282532.2:c.2617G>T | NP_001269461.1:p.Asp873Tyr |