Linked Data
ClinVar Variation Id:
515383
dbSNP Id:
rs371972266
ExAC:
19:13325119 G / A
gnomAD v2:
19-13325119-G-A
gnomAD v3:
19-13214305-G-A
gnomAD v4:
19-13214305-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.13214305G>A , CM000681.2:g.13214305G>A | GRCh38 |
| NC_000019.9:g.13325119G>A , CM000681.1:g.13325119G>A | GRCh37 |
| NC_000019.8:g.13186119G>A | NCBI36 |
| NG_011569.1:g.297156C>T , LRG_7:g.297156C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360228.11:c.5868C>T MANE Select | ENSP00000353362.5:p.Tyr1956= | |
| ENST00000573710.7:c.5874C>T | ENSP00000460092.3:p.Tyr1958= | |
| ENST00000585802.6:c.1029C>T | ENSP00000465598.2:p.Tyr343= | |
| ENST00000635727.1:c.5871C>T | ENSP00000490001.1:p.Tyr1957= | |
| ENST00000635895.1:c.5871C>T | ENSP00000490323.1:p.Tyr1957= | |
| ENST00000635988.1:n.2026C>T | ||
| ENST00000636012.1:c.5871C>T | ENSP00000490223.1:p.Tyr1957= | |
| ENST00000636074.1:n.930C>T | ||
| ENST00000636389.1:c.5871C>T | ENSP00000489992.1:p.Tyr1957= | |
| ENST00000636473.1:c.738C>T | ENSP00000490173.1:p.Tyr246= | |
| ENST00000636549.1:c.5877C>T | ENSP00000490578.1:p.Tyr1959= | |
| ENST00000636610.1:n.785C>T | ||
| ENST00000636768.1:c.398C>T | ENSP00000490190.1:n.398C>T | |
| ENST00000637276.1:c.5871C>T | ENSP00000489777.1:p.Tyr1957= | |
| ENST00000637432.1:c.5886C>T | ENSP00000490617.1:p.Tyr1962= | |
| ENST00000637736.1:c.5730C>T | ENSP00000489861.1:p.Tyr1910= | |
| ENST00000637769.1:c.5871C>T | ENSP00000489778.1:p.Tyr1957= | |
| ENST00000637819.1:c.1272C>T | ENSP00000490686.1:p.Tyr424= | |
| ENST00000637927.1:c.5874C>T | ENSP00000489715.1:p.Tyr1958= | |
| ENST00000638009.2:c.5871C>T | ENSP00000489913.1:p.Tyr1957= | |
| ENST00000638029.1:c.5886C>T | ENSP00000489829.1:p.Tyr1962= | |
| ENST00000638114.1:n.80C>T | ||
| ENST00000664864.1:c.6072C>T | ENSP00000499449.1:p.Tyr2024= | |
| ENST00000360228.9:c.5868C>T | ENSP00000353362.5:p.Tyr1956= | |
| ENST00000573710.6:c.5871C>T | ENSP00000460092.2:p.Tyr1957= | |
| ENST00000585802.5:c.1926C>T | ENSP00000465598.1:p.Tyr642= | |
| ENST00000587525.5:c.1329C>T | ENSP00000467729.1:p.Tyr443= | |
| ENST00000614285.4:c.5886C>T | ENSP00000479983.1:p.Tyr1962= | |
| NM_000068.3:c.5886C>T | NP_000059.3:p.Tyr1962= | |
| NM_001127221.1:c.5871C>T , LRG_7t1:c.5871C>T | NP_001120693.1:p.Tyr1957= | |
| NM_001127222.1:c.5868C>T | NP_001120694.1:p.Tyr1956= | |
| NM_001174080.1:c.5877C>T | NP_001167551.1:p.Tyr1959= | |
| NM_023035.2:c.5886C>T | NP_075461.2:p.Tyr1962= | |
| NM_000068.4:c.5886C>T | NP_000059.3:p.Tyr1962= | |
| NM_001127222.2:c.5868C>T MANE Select | NP_001120694.1:p.Tyr1956= | |
| NM_001174080.2:c.5877C>T | NP_001167551.1:p.Tyr1959= | |
| NM_023035.3:c.5886C>T | NP_075461.2:p.Tyr1962= | |
| NM_001127221.2:c.5871C>T | NP_001120693.1:p.Tyr1957= |