Linked Data
ClinVar Variation Id:
330446
dbSNP Id:
rs886054687
gnomAD v2:
19-7125498-C-T
gnomAD v4:
19-7125487-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7125487C>T , CM000681.2:g.7125487C>T | GRCh38 |
| NC_000019.9:g.7125498C>T , CM000681.1:g.7125498C>T | GRCh37 |
| NC_000019.8:g.7076498C>T | NCBI36 |
| NG_008852.2:g.173514G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.3054G>A MANE Select | ENSP00000303830.4:p.Val1018= | |
| ENST00000302850.9:c.3054G>A | ENSP00000303830.4:p.Val1018= | |
| ENST00000341500.9:c.3018G>A | ENSP00000342838.4:p.Val1006= | |
| NM_000208.2:c.3054G>A | NP_000199.2:p.Val1018= | |
| NM_000208.3:c.3054G>A | NP_000199.2:p.Val1018= | |
| NM_001079817.1:c.3018G>A | NP_001073285.1:p.Val1006= | |
| NM_001079817.2:c.3018G>A | NP_001073285.1:p.Val1006= | |
| XM_011527988.1:c.3129G>A | XP_011526290.1:p.Val1043= | |
| XM_011527989.1:c.3093G>A | XP_011526291.1:p.Val1031= | |
| XM_011527988.2:c.3051G>A | XP_011526290.2:p.Val1017= | |
| XM_011527989.3:c.3015G>A | XP_011526291.2:p.Val1005= | |
| NM_000208.4:c.3054G>A MANE Select | NP_000199.2:p.Val1018= | |
| NM_001079817.3:c.3018G>A | NP_001073285.1:p.Val1006= |