Linked Data
ClinVar Variation Id:
2893686
dbSNP Id:
rs1974408024
gnomAD v3:
19-38585035-C-T
gnomAD v4:
19-38585035-C-T
MyVariant Identifiers:
chr19:g.39075675C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38585035C>T , CM000681.2:g.38585035C>T | GRCh38 |
| NC_000019.9:g.39075675C>T , CM000681.1:g.39075675C>T | GRCh37 |
| NC_000019.8:g.43767515C>T | NCBI36 |
| NG_008866.1:g.156336C>T , LRG_766:g.156336C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000593677.2:c.1675C>T | ||
| ENST00000688602.1:c.3072C>T | ||
| ENST00000689936.1:c.3044C>T | ||
| ENST00000692547.1:n.132C>T | ||
| ENST00000359596.8:c.14739C>T MANE Select | ENSP00000352608.2:p.Tyr4913= | |
| ENST00000355481.8:c.14724C>T | ENSP00000347667.3:p.Tyr4908= | |
| ENST00000359596.7:c.14739C>T | ENSP00000352608.2:p.Tyr4913= | |
| ENST00000360985.7:c.14721C>T | ENSP00000354254.4:p.Tyr4907= | |
| NM_000540.2:c.14739C>T , LRG_766t1:c.14739C>T | NP_000531.2:p.Tyr4913= | |
| NM_001042723.1:c.14724C>T | NP_001036188.1:p.Tyr4908= | |
| XM_006723317.1:c.14721C>T | XP_006723380.1:p.Tyr4907= | |
| XM_006723319.1:c.14706C>T | XP_006723382.1:p.Tyr4902= | |
| XM_011527204.1:c.14736C>T | XP_011525506.1:p.Tyr4912= | |
| XM_011527205.1:c.14652C>T | XP_011525507.1:p.Tyr4884= | |
| XM_006723317.2:c.14721C>T | XP_006723380.1:p.Tyr4907= | |
| XM_006723319.2:c.14706C>T | XP_006723382.1:p.Tyr4902= | |
| XM_011527205.2:c.14652C>T | XP_011525507.1:p.Tyr4884= | |
| NM_000540.3:c.14739C>T MANE Select | NP_000531.2:p.Tyr4913= | |
| NM_001042723.2:c.14724C>T | NP_001036188.1:p.Tyr4908= |