Linked Data
ClinVar Variation Id:
2860764
ClinVar RCV Id:
RCV003697038
dbSNP Id:
rs727504937
gnomAD v3:
2-26460151-G-T
gnomAD v4:
2-26460151-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26460151G>T , CM000664.2:g.26460151G>T | GRCh38 |
| NC_000002.11:g.26683019G>T , CM000664.1:g.26683019G>T | GRCh37 |
| NC_000002.10:g.26536523G>T | NCBI36 |
| NG_009937.1:g.103548C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.5868C>A MANE Select | ENSP00000272371.2:p.Tyr1956Ter | |
| ENST00000339598.8:c.3512+496C>A MANE Plus Clinical | ENSP00000344521.3:n.3512+496C>A | |
| ENST00000402415.8:c.3627C>A | ENSP00000383906.4:p.Tyr1209Ter | |
| ENST00000272371.6:c.5868C>A | ENSP00000272371.2:p.Tyr1956Ter | |
| ENST00000338581.10:c.3567C>A | ENSP00000345137.6:p.Tyr1189Ter | |
| ENST00000339598.7:c.3512+496C>A | ENSP00000344521.3:n.3512+496C>A | |
| ENST00000402415.7:c.3798C>A | ENSP00000383906.3:p.Tyr1266Ter | |
| ENST00000403946.7:c.5813+496C>A | ENSP00000385255.3:n.5813+496C>A | |
| NM_001287489.1:c.5813+496C>A | NP_001274418.1:n.5813+496C>A | |
| NM_004802.3:c.3567C>A | NP_004793.2:p.Tyr1189Ter | |
| NM_194248.2:c.5868C>A | NP_919224.1:p.Tyr1956Ter | |
| NM_194322.2:c.3798C>A | NP_919303.1:p.Tyr1266Ter | |
| NM_194323.2:c.3512+496C>A | NP_919304.1:n.3512+496C>A | |
| XM_005264644.2:c.5798+496C>A | XP_005264701.1:n.5798+496C>A | |
| XM_011533185.1:c.5858+496C>A | XP_011531487.1:n.5858+496C>A | |
| XM_017005338.1:c.5808C>A | XP_016860827.1:p.Tyr1936Ter | |
| NM_001287489.2:c.5813+496C>A | NP_001274418.1:n.5813+496C>A | |
| NM_004802.4:c.3567C>A | NP_004793.2:p.Tyr1189Ter | |
| NM_194248.3:c.5868C>A MANE Select | NP_919224.1:p.Tyr1956Ter | |
| NM_194322.3:c.3798C>A | NP_919303.1:p.Tyr1266Ter | |
| NM_194323.3:c.3512+496C>A MANE Plus Clinical | NP_919304.1:n.3512+496C>A |