Linked Data
ClinVar Variation Id:
254708
dbSNP Id:
rs115378744
ExAC:
12:52310026 C / T
gnomAD v2:
12-52310026-C-T
gnomAD v3:
12-51916242-C-T
gnomAD v4:
12-51916242-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51916242C>T , CM000674.2:g.51916242C>T | GRCh38 |
| NC_000012.11:g.52310026C>T , CM000674.1:g.52310026C>T | GRCh37 |
| NC_000012.10:g.50596293C>T | NCBI36 |
| NG_009549.1:g.13825C>T , LRG_543:g.13825C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000547400.6:c.976+9C>T | ENSP00000446724.2:n.976+9C>T | |
| ENST00000551576.6:c.1246+9C>T | ENSP00000455848.2:n.1246+9C>T | |
| ENST00000552678.2:c.1246+9C>T | ENSP00000457394.2:n.1246+9C>T | |
| ENST00000388922.9:c.1246+9C>T MANE Select | ENSP00000373574.4:n.1246+9C>T | |
| ENST00000388922.8:c.1246+9C>T | ENSP00000373574.4:n.1246+9C>T | |
| ENST00000419526.6:c.724+9C>T | ENSP00000392492.2:n.724+9C>T | |
| ENST00000547632.1:n.521+9C>T | ||
| ENST00000550683.5:c.1288+9C>T | ENSP00000447884.1:n.1288+9C>T | |
| ENST00000552678.1:c.251+9C>T | ||
| NM_000020.2:c.1246+9C>T , LRG_543t1:c.1246+9C>T | NP_000011.2:n.1246+9C>T | |
| NM_001077401.1:c.1246+9C>T | NP_001070869.1:n.1246+9C>T | |
| XM_005269235.2:c.1246+9C>T | XP_005269292.1:n.1246+9C>T | |
| XM_011539008.1:c.976+9C>T | XP_011537310.1:n.976+9C>T | |
| XM_024449279.1:c.457+9C>T | XP_024305047.1:n.457+9C>T | |
| NM_000020.3:c.1246+9C>T MANE Select | NP_000011.2:n.1246+9C>T | |
| NM_001077401.2:c.1246+9C>T | NP_001070869.1:n.1246+9C>T |