Linked Data
ClinVar Variation Id:
2716081
ClinVar RCV Id:
RCV003534147
dbSNP Id:
rs368442419
ExAC:
9:35092627 C / T
gnomAD v2:
9-35092627-C-T
gnomAD v3:
9-35092630-C-T
gnomAD v4:
9-35092630-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.35092630C>T , CM000671.2:g.35092630C>T | GRCh38 |
| NC_000009.11:g.35092627C>T , CM000671.1:g.35092627C>T | GRCh37 |
| NC_000009.10:g.35082627C>T | NCBI36 |
| NG_031990.1:g.8972G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361778.7:c.1257G>A | ENSP00000354678.2:p.Ala419= | |
| ENST00000700254.1:c.1257G>A | ENSP00000514892.1:p.Ala419= | |
| ENST00000700255.1:c.*437G>A | ENSP00000514893.1:n.*437G>A | |
| ENST00000700256.1:n.1289G>A | ||
| ENST00000700257.1:c.1257G>A | ENSP00000514894.1:p.Ala419= | |
| ENST00000700259.1:c.1257G>A | ENSP00000514895.1:p.Ala419= | |
| ENST00000700260.1:c.1077G>A | ENSP00000514896.1:p.Ala359= | |
| ENST00000700261.1:c.1257G>A | ENSP00000514897.1:p.Ala419= | |
| ENST00000700262.1:c.1257G>A | ENSP00000514898.1:p.Ala419= | |
| ENST00000700263.1:c.1133G>A | ENSP00000514899.1:n.1133G>A | |
| ENST00000700264.1:c.1257G>A | ENSP00000514900.1:p.Ala419= | |
| ENST00000378617.4:c.1257G>A MANE Select | ENSP00000367880.3:p.Ala419= | |
| ENST00000298004.9:c.1257G>A | ENSP00000298004.5:p.Ala419= | |
| ENST00000361778.6:c.1257G>A | ENSP00000354678.2:p.Ala419= | |
| ENST00000378617.3:c.1257G>A | ENSP00000367880.3:p.Ala419= | |
| ENST00000465745.6:n.2258G>A | ||
| ENST00000474436.1:n.2715G>A | ||
| NM_001201484.1:c.1257G>A | NP_001188413.1:p.Ala419= | |
| NM_032634.3:c.1257G>A | NP_116023.2:p.Ala419= | |
| NM_152850.3:c.1257G>A | NP_690577.2:p.Ala419= | |
| XM_005251619.2:c.1257G>A | XP_005251676.1:p.Ala419= | |
| XM_011518056.1:c.1257G>A | XP_011516358.1:p.Ala419= | |
| XR_242515.1:n.1278G>A | ||
| XM_005251619.3:c.1257G>A | XP_005251676.1:p.Ala419= | |
| XM_017015222.2:c.1257G>A | XP_016870711.1:p.Ala419= | |
| XM_017015223.1:c.1257G>A | XP_016870712.1:p.Ala419= | |
| XM_017015224.1:c.1257G>A | XP_016870713.1:p.Ala419= | |
| XR_001746390.1:n.1680G>A | ||
| XR_001746391.2:n.1278G>A | ||
| XR_242515.3:n.1278G>A | ||
| NM_032634.4:c.1257G>A MANE Select | NP_116023.2:p.Ala419= | |
| NM_001201484.2:c.1257G>A | NP_001188413.1:p.Ala419= | |
| NM_152850.4:c.1257G>A | NP_690577.2:p.Ala419= |