Linked Data
ClinVar Variation Id:
1111674
dbSNP Id:
rs2126589832
gnomAD v4:
5-236493-C-T
MyVariant Identifiers:
chr5:g.236608C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.236493C>T , CM000667.2:g.236493C>T | GRCh38 |
| NC_000005.9:g.236608C>T , CM000667.1:g.236608C>T | GRCh37 |
| NC_000005.8:g.289608C>T | NCBI36 |
| NG_012339.1:g.23253C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264932.11:c.1326C>T MANE Select | ENSP00000264932.6:p.Ala442= | |
| ENST00000651543.1:c.*59C>T | ENSP00000499215.1:n.*59C>T | |
| ENST00000264932.10:c.1326C>T | ENSP00000264932.6:p.Ala442= | |
| ENST00000504309.5:c.1326C>T | ENSP00000426514.1:p.Ala442= | |
| ENST00000505555.5:n.1366C>T | ||
| ENST00000510361.5:c.1182C>T | ENSP00000427703.1:p.Ala394= | |
| ENST00000511810.5:n.2073C>T | ||
| ENST00000512962.5:n.912C>T | ||
| ENST00000514027.5:n.1281C>T | ||
| ENST00000515752.5:n.912C>T | ||
| ENST00000617470.4:c.891C>T | ENSP00000484230.1:p.Ala297= | |
| NM_001294332.1:c.1182C>T | NP_001281261.1:p.Ala394= | |
| NM_004168.3:c.1326C>T | NP_004159.2:p.Ala442= | |
| XM_005248331.2:c.1326C>T | XP_005248388.1:p.Ala442= | |
| XM_011514072.1:c.1326C>T | XP_011512374.1:p.Ala442= | |
| XM_011514073.1:c.1326C>T | XP_011512375.1:p.Ala442= | |
| XR_925638.1:n.1459C>T | ||
| NM_001330758.1:c.1326C>T | NP_001317687.1:p.Ala442= | |
| XM_011514072.2:c.1326C>T | XP_011512374.1:p.Ala442= | |
| XM_011514073.2:c.1326C>T | XP_011512375.1:p.Ala442= | |
| XM_017009685.2:c.1326C>T | XP_016865174.1:p.Ala442= | |
| XM_024446143.1:c.1182C>T | XP_024301911.1:p.Ala394= | |
| XR_002956167.1:n.1373C>T | ||
| NM_004168.4:c.1326C>T MANE Select | NP_004159.2:p.Ala442= | |
| NM_001294332.2:c.1182C>T | NP_001281261.1:p.Ala394= | |
| NM_001330758.2:c.1326C>T | NP_001317687.1:p.Ala442= |