Linked Data
ClinVar Variation Id:
1668967
ClinVar RCV Id:
RCV002194346
dbSNP Id:
rs770691939
gnomAD v3:
6-149370116-T-G
gnomAD v4:
6-149370116-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.149370116T>G , CM000668.2:g.149370116T>G | GRCh38 |
| NC_000006.11:g.149691252T>G , CM000668.1:g.149691252T>G | GRCh37 |
| NC_000006.10:g.149732945T>G | NCBI36 |
| NG_021386.1:g.56817T>G | |
| NG_021386.2:g.157193T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703212.1:n.517+17T>G | ||
| ENST00000703213.1:c.102+17T>G | ENSP00000515239.1:n.102+17T>G | |
| ENST00000636456.1:c.-96-8556T>G | ENSP00000490379.1:n.-96-8556T>G | |
| ENST00000637181.2:c.102+17T>G MANE Select | ENSP00000490618.1:n.102+17T>G | |
| ENST00000367456.5:c.102+17T>G | ENSP00000356426.1:n.102+17T>G | |
| ENST00000470466.5:c.102+17T>G | ENSP00000432709.1:n.102+17T>G | |
| ENST00000538427.5:c.102+17T>G | ENSP00000445752.1:n.102+17T>G | |
| ENST00000606202.1:c.-120-7902T>G | ENSP00000476139.1:n.-120-7902T>G | |
| ENST00000606797.5:c.78+41T>G | ENSP00000475580.1:n.78+41T>G | |
| NM_001292034.2:c.102+17T>G | NP_001278963.1:n.102+17T>G | |
| NM_001292035.2:c.7-7902T>G | NP_001278964.1:n.7-7902T>G | |
| NM_015093.5:c.102+17T>G | NP_055908.1:n.102+17T>G | |
| XM_006715403.2:c.102+17T>G | XP_006715466.1:n.102+17T>G | |
| XM_011535633.1:c.102+17T>G | XP_011533935.1:n.102+17T>G | |
| XM_011535634.1:c.102+17T>G | XP_011533936.1:n.102+17T>G | |
| XM_011535633.2:c.102+17T>G | XP_011533935.1:n.102+17T>G | |
| XM_017010591.1:c.102+17T>G | XP_016866080.1:n.102+17T>G | |
| XM_017010592.2:c.102+17T>G | XP_016866081.1:n.102+17T>G | |
| NM_001292034.3:c.102+17T>G MANE Select | NP_001278963.1:n.102+17T>G | |
| NM_001292035.3:c.7-7902T>G | NP_001278964.1:n.7-7902T>G | |
| NM_001369506.1:c.102+17T>G | NP_001356435.1:n.102+17T>G | |
| NM_015093.6:c.102+17T>G | NP_055908.1:n.102+17T>G |