Linked Data
dbSNP Id:
rs113368668
ExAC:
11:67815327 G / T
gnomAD v2:
11-67815327-G-T
gnomAD v3:
11-68047860-G-T
gnomAD v4:
11-68047860-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.68047860G>T , CM000673.2:g.68047860G>T | GRCh38 |
| NC_000011.9:g.67815327G>T , CM000673.1:g.67815327G>T | GRCh37 |
| NC_000011.8:g.67571903G>T | NCBI36 |
| NG_007878.1:g.13845G>T , LRG_115:g.13845G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530449.2:n.89-22G>T | ||
| ENST00000698254.1:c.993-22G>T | ENSP00000513629.1:n.993-22G>T | |
| ENST00000698255.1:c.1413-22G>T | ENSP00000513630.1:n.1413-22G>T | |
| ENST00000698256.1:c.930-22G>T | ||
| ENST00000698257.1:n.882-22G>T | ||
| ENST00000698258.1:n.577G>T | ||
| ENST00000698259.1:n.343G>T | ||
| ENST00000265686.8:c.1464-22G>T MANE Select | ENSP00000265686.3:n.1464-22G>T | |
| ENST00000265686.7:c.1464-22G>T | ENSP00000265686.3:n.1464-22G>T | |
| ENST00000525516.1:n.258-22G>T | ||
| ENST00000525724.5:n.776-22G>T | ||
| ENST00000528981.5:c.616-22G>T | ||
| ENST00000532635.5:c.816-22G>T | ENSP00000434407.1:n.816-22G>T | |
| ENST00000533005.5:n.555G>T | ||
| NM_006019.3:c.1464-22G>T | NP_006010.2:n.1464-22G>T | |
| NM_006053.3:c.816-22G>T | NP_006044.1:n.816-22G>T | |
| XM_005273709.2:c.1464-22G>T | XP_005273766.1:n.1464-22G>T | |
| XM_011544726.1:c.1464-22G>T | XP_011543028.1:n.1464-22G>T | |
| XM_011544727.1:c.1464-22G>T | XP_011543029.1:n.1464-22G>T | |
| XM_011544728.1:c.1464-22G>T | XP_011543030.1:n.1464-22G>T | |
| XM_011544729.1:c.1480-22G>T | XP_011543031.1:n.1480-22G>T | |
| XR_949754.1:n.1468-22G>T | ||
| NM_001351059.1:c.570-22G>T | NP_001337988.1:n.570-22G>T | |
| XM_024448320.1:c.1535G>T | XP_024304088.1:p.Arg512Leu | |
| XM_024448321.1:c.1535G>T | XP_024304089.1:p.Arg512Leu | |
| XM_024448322.1:c.1535G>T | XP_024304090.1:p.Arg512Leu | |
| XM_024448323.1:c.1535G>T | XP_024304091.1:p.Arg512Leu | |
| XM_024448324.1:c.1535G>T | XP_024304092.1:p.Arg512Leu | |
| XR_001747721.2:n.1588-22G>T | ||
| XR_001747722.1:n.1601-22G>T | ||
| XR_001747723.2:n.1601-22G>T | ||
| XR_002957115.1:n.1657G>T | ||
| NM_006019.4:c.1464-22G>T MANE Select | NP_006010.2:n.1464-22G>T | |
| NM_001351059.2:c.570-22G>T | NP_001337988.1:n.570-22G>T | |
| NM_006053.4:c.816-22G>T | NP_006044.1:n.816-22G>T |