Linked Data
ClinVar Variation Id:
983635
dbSNP Id:
rs752094219
ExAC:
6:129618992 C / T
gnomAD v3:
6-129297847-C-T
gnomAD v4:
6-129297847-C-T
MyVariant Identifiers:
chr6:g.129618992C>T (hg19)
chr6:g.129618992_129618994delinsTAA (hg19)
chr6:g.129297847C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129297847C>T , CM000668.2:g.129297847C>T | GRCh38 |
| NC_000006.11:g.129618992C>T , CM000668.1:g.129618992C>T | GRCh37 |
| NC_000006.10:g.129660685C>T | NCBI36 |
| NG_008678.1:g.419707C>T , LRG_409:g.419707C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617695.5:c.3019C>T | ENSP00000481744.2:p.Gln1007Ter | |
| ENST00000618192.5:c.3283C>T | ENSP00000480802.2:p.Gln1095Ter | |
| ENST00000421865.3:c.3019C>T MANE Select | ENSP00000400365.2:p.Gln1007Ter | |
| ENST00000645154.1:c.534C>T | ||
| ENST00000421865.2:c.3019C>T | ENSP00000400365.2:p.Gln1007Ter | |
| ENST00000617695.4:c.3019C>T | ENSP00000481744.1:p.Gln1007Ter | |
| ENST00000618192.4:c.3019C>T | ENSP00000480802.1:p.Gln1007Ter | |
| NM_000426.3:c.3019C>T , LRG_409t1:c.3019C>T | NP_000417.2:p.Gln1007Ter | |
| NM_001079823.1:c.3019C>T | NP_001073291.1:p.Gln1007Ter | |
| XM_005266981.2:c.3283C>T | XP_005267038.1:p.Gln1095Ter | |
| XM_005266982.2:c.3283C>T | XP_005267039.1:p.Gln1095Ter | |
| XM_011535820.1:c.3283C>T | XP_011534122.1:p.Gln1095Ter | |
| XM_005266981.3:c.3283C>T | XP_005267038.1:p.Gln1095Ter | |
| XM_005266982.3:c.3283C>T | XP_005267039.1:p.Gln1095Ter | |
| XM_011535820.2:c.3283C>T | XP_011534122.1:p.Gln1095Ter | |
| XM_017010851.2:c.3289C>T | XP_016866340.1:p.Gln1097Ter | |
| XM_017010852.1:c.1414C>T | XP_016866341.1:p.Gln472Ter | |
| XM_017010853.1:c.3283C>T | XP_016866342.1:p.Gln1095Ter | |
| NM_000426.4:c.3019C>T MANE Select | NP_000417.3:p.Gln1007Ter | |
| NM_001079823.2:c.3019C>T | NP_001073291.2:p.Gln1007Ter |