Linked Data
ClinVar Variation Id:
811204
ClinVar RCV Id:
RCV001000915
dbSNP Id:
rs1592223964
gnomAD v4:
12-51915222-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51915222C>G , CM000674.2:g.51915222C>G | GRCh38 |
| NC_000012.11:g.52309006C>G , CM000674.1:g.52309006C>G | GRCh37 |
| NC_000012.10:g.50595273C>G | NCBI36 |
| NG_009549.1:g.12805C>G , LRG_543:g.12805C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000547400.6:c.503-3C>G | ENSP00000446724.2:n.503-3C>G | |
| ENST00000551576.6:c.773-3C>G | ENSP00000455848.2:n.773-3C>G | |
| ENST00000552678.2:c.773-3C>G | ENSP00000457394.2:n.773-3C>G | |
| ENST00000388922.9:c.773-3C>G MANE Select | ENSP00000373574.4:n.773-3C>G | |
| ENST00000388922.8:c.773-3C>G | ENSP00000373574.4:n.773-3C>G | |
| ENST00000419526.6:c.251-3C>G | ENSP00000392492.2:n.251-3C>G | |
| ENST00000550683.5:c.815-3C>G | ENSP00000447884.1:n.815-3C>G | |
| NM_000020.2:c.773-3C>G , LRG_543t1:c.773-3C>G | NP_000011.2:n.773-3C>G | |
| NM_001077401.1:c.773-3C>G | NP_001070869.1:n.773-3C>G | |
| XM_005269235.2:c.773-3C>G | XP_005269292.1:n.773-3C>G | |
| XM_011539008.1:c.503-3C>G | XP_011537310.1:n.503-3C>G | |
| XM_024449279.1:c.-17-3C>G | XP_024305047.1:n.-17-3C>G | |
| NM_000020.3:c.773-3C>G MANE Select | NP_000011.2:n.773-3C>G | |
| NM_001077401.2:c.773-3C>G | NP_001070869.1:n.773-3C>G |