Linked Data
ClinVar Variation Id:
2173108
dbSNP Id:
rs1294294978
gnomAD v3:
19-38564988-C-T
gnomAD v4:
19-38564988-C-T
COSMIC:
COSM188801
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38564988C>T , CM000681.2:g.38564988C>T | GRCh38 |
| NC_000019.9:g.39055628C>T , CM000681.1:g.39055628C>T | GRCh37 |
| NC_000019.8:g.43747468C>T | NCBI36 |
| NG_008866.1:g.136289C>T , LRG_766:g.136289C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000688602.1:c.1064C>T | ||
| ENST00000689936.1:c.1046C>T | ||
| ENST00000359596.8:c.12654C>T MANE Select | ENSP00000352608.2:p.Phe4218= | |
| ENST00000355481.8:c.12639C>T | ENSP00000347667.3:p.Phe4213= | |
| ENST00000359596.7:c.12654C>T | ENSP00000352608.2:p.Phe4218= | |
| ENST00000360985.7:c.12636C>T | ENSP00000354254.4:p.Phe4212= | |
| ENST00000594335.5:c.6023C>T | ||
| NM_000540.2:c.12654C>T , LRG_766t1:c.12654C>T | NP_000531.2:p.Phe4218= | |
| NM_001042723.1:c.12639C>T | NP_001036188.1:p.Phe4213= | |
| XM_006723317.1:c.12636C>T | XP_006723380.1:p.Phe4212= | |
| XM_006723319.1:c.12621C>T | XP_006723382.1:p.Phe4207= | |
| XM_011527204.1:c.12651C>T | XP_011525506.1:p.Phe4217= | |
| XM_011527205.1:c.12654C>T | XP_011525507.1:p.Phe4218= | |
| XM_006723317.2:c.12636C>T | XP_006723380.1:p.Phe4212= | |
| XM_006723319.2:c.12621C>T | XP_006723382.1:p.Phe4207= | |
| XM_011527205.2:c.12654C>T | XP_011525507.1:p.Phe4218= | |
| NM_000540.3:c.12654C>T MANE Select | NP_000531.2:p.Phe4218= | |
| NM_001042723.2:c.12639C>T | NP_001036188.1:p.Phe4213= |