Linked Data
ClinVar Variation Id:
11290
ClinVar RCV Id:
RCV000012042
dbSNP Id:
rs128627257
PubMed:
PMID:17024373
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32310214A>C , CM000685.2:g.32310214A>C | GRCh38 |
| NC_000023.10:g.32328331A>C , CM000685.1:g.32328331A>C | GRCh37 |
| NC_000023.9:g.32238252A>C | NCBI36 |
| NG_012232.1:g.1034396T>G , LRG_199:g.1034396T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.831T>G | ENSP00000350765.3:p.Tyr277Ter | |
| ENST00000357033.9:c.5985T>G MANE Select | ENSP00000354923.3:p.Tyr1995Ter | |
| ENST00000619831.5:c.1953T>G | ENSP00000479270.2:p.Tyr651Ter | |
| ENST00000357033.8:c.5985T>G | ENSP00000354923.3:p.Tyr1995Ter | |
| ENST00000378677.6:c.5973T>G | ENSP00000367948.2:p.Tyr1991Ter | |
| ENST00000488902.5:n.336-93151T>G | ||
| ENST00000619831.4:c.5973T>G | ENSP00000479270.1:p.Tyr1991Ter | |
| ENST00000620040.4:c.5985T>G | ENSP00000478150.1:p.Tyr1995Ter | |
| NM_000109.3:c.5961T>G | NP_000100.2:p.Tyr1987Ter | |
| NM_004006.2:c.5985T>G , LRG_199t1:c.5985T>G | NP_003997.1:p.Tyr1995Ter | |
| NM_004009.3:c.5973T>G | NP_004000.1:p.Tyr1991Ter | |
| NM_004010.3:c.5616T>G | NP_004001.1:p.Tyr1872Ter | |
| NM_004011.3:c.1962T>G | NP_004002.2:p.Tyr654Ter | |
| NM_004012.3:c.1953T>G | NP_004003.1:p.Tyr651Ter | |
| XM_006724468.2:c.5985T>G | XP_006724531.1:p.Tyr1995Ter | |
| XM_006724469.2:c.5961T>G | XP_006724532.1:p.Tyr1987Ter | |
| XM_006724470.2:c.5985T>G | XP_006724533.1:p.Tyr1995Ter | |
| XM_006724471.2:c.5985T>G | XP_006724534.1:p.Tyr1995Ter | |
| XM_006724472.2:c.5856T>G | XP_006724535.1:p.Tyr1952Ter | |
| XM_006724473.2:c.5847T>G | XP_006724536.1:p.Tyr1949Ter | |
| XM_006724474.2:c.5985T>G | XP_006724537.1:p.Tyr1995Ter | |
| XM_006724475.2:c.5985T>G | XP_006724538.1:p.Tyr1995Ter | |
| XM_011545467.1:c.5862T>G | XP_011543769.1:p.Tyr1954Ter | |
| XM_011545468.1:c.5985T>G | XP_011543770.1:p.Tyr1995Ter | |
| XM_006724469.3:c.5961T>G | XP_006724532.1:p.Tyr1987Ter | |
| XM_006724470.3:c.5985T>G | XP_006724533.1:p.Tyr1995Ter | |
| XM_006724474.3:c.5985T>G | XP_006724537.1:p.Tyr1995Ter | |
| XM_011545468.2:c.5985T>G | XP_011543770.1:p.Tyr1995Ter | |
| XM_017029328.1:c.5985T>G | XP_016884817.1:p.Tyr1995Ter | |
| XM_017029329.1:c.5985T>G | XP_016884818.1:p.Tyr1995Ter | |
| XM_017029330.2:c.5985T>G | XP_016884819.1:p.Tyr1995Ter | |
| XM_017029331.1:c.159T>G | XP_016884820.1:p.Tyr53Ter | |
| NM_000109.4:c.5961T>G | NP_000100.3:p.Tyr1987Ter | |
| NM_004006.3:c.5985T>G MANE Select | NP_003997.2:p.Tyr1995Ter | |
| NM_004011.4:c.1962T>G | NP_004002.3:p.Tyr654Ter | |
| NM_004012.4:c.1953T>G | NP_004003.2:p.Tyr651Ter |