Linked Data
ClinVar Variation Id:
385632
dbSNP Id:
rs567406924
gnomAD v2:
12-124229269-C-T
gnomAD v3:
12-123744722-C-T
gnomAD v4:
12-123744722-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.123744722C>T , CM000674.2:g.123744722C>T | GRCh38 |
| NC_000012.11:g.124229269C>T , CM000674.1:g.124229269C>T | GRCh37 |
| NC_000012.10:g.122795222C>T | NCBI36 |
| NG_012743.1:g.37405C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000330342.8:c.1452C>T MANE Select | ENSP00000332247.2:p.Asn484= | |
| ENST00000540368.6:n.1483C>T | ||
| ENST00000674794.1:c.1540C>T | ||
| ENST00000675260.1:n.727C>T | ||
| ENST00000675344.1:c.*473C>T | ENSP00000501953.1:n.*473C>T | |
| ENST00000330342.7:c.1452C>T | ENSP00000332247.2:p.Asn484= | |
| ENST00000536426.1:n.469C>T | ||
| ENST00000545059.5:n.4088C>T | ||
| NM_012463.3:c.1452C>T | NP_036595.2:p.Asn484= | |
| XM_005253563.1:c.1452C>T | XP_005253620.1:p.Asn484= | |
| XM_006719317.2:c.939C>T | XP_006719380.1:p.Asn313= | |
| XM_006719318.2:c.630C>T | XP_006719381.1:p.Asn210= | |
| XR_429088.1:n.1615C>T | ||
| XM_024448910.1:c.1452C>T | XP_024304678.1:p.Asn484= | |
| XM_024448911.1:c.939C>T | XP_024304679.1:p.Asn313= | |
| XM_024448912.1:c.630C>T | XP_024304680.1:p.Asn210= | |
| NM_012463.4:c.1452C>T MANE Select | NP_036595.2:p.Asn484= |