Linked Data
dbSNP Id:
rs1136695
gnomAD v4:
6-29943287-A-T
MyVariant Identifiers:
chr6:g.29911064A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.29943287A>T , CM000668.2:g.29943287A>T | GRCh38 |
| NC_000006.11:g.29911064A>T , CM000668.1:g.29911064A>T | GRCh37 |
| NC_000006.10:g.30019043A>T | NCBI36 |
| NG_029217.2:g.5822A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638375.2:c.363A>T | ENSP00000492789.2:p.Ile121= | |
| ENST00000706892.1:n.639A>T | ||
| ENST00000706893.1:c.363A>T | ENSP00000516609.1:p.Ile121= | |
| ENST00000706894.1:c.363A>T | ENSP00000516610.1:p.Ile121= | |
| ENST00000706895.1:n.639A>T | ||
| ENST00000706896.1:n.639A>T | ||
| ENST00000706897.1:n.639A>T | ||
| ENST00000706898.1:c.363A>T | ENSP00000516611.1:p.Ile121= | |
| ENST00000706899.1:n.639A>T | ||
| ENST00000706900.1:c.279A>T | ENSP00000516617.1:p.Ile93= | |
| ENST00000706901.1:c.363A>T | ENSP00000516612.1:p.Ile121= | |
| ENST00000706902.1:c.363A>T | ENSP00000516613.1:p.Ile121= | |
| ENST00000706903.1:c.363A>T | ENSP00000516614.1:p.Ile121= | |
| ENST00000706904.1:c.363A>T | ENSP00000516615.1:p.Ile121= | |
| ENST00000706905.1:c.363A>T | ENSP00000516616.1:p.Ile121= | |
| ENST00000376809.10:c.363A>T MANE Select | ENSP00000366005.5:p.Ile121= | |
| ENST00000638375.1:c.363A>T | ENSP00000492789.1:p.Ile121= | |
| ENST00000376802.2:c.363A>T | ENSP00000365998.2:p.Ile121= | |
| ENST00000376806.9:c.363A>T | ENSP00000366002.5:p.Ile121= | |
| ENST00000376809.9:c.363A>T | ENSP00000366005.5:p.Ile121= | |
| ENST00000396634.5:c.363A>T | ENSP00000379873.1:p.Ile121= | |
| ENST00000461903.1:n.604A>T | ||
| ENST00000479320.5:n.604A>T | ||
| ENST00000495183.5:n.606A>T | ||
| ENST00000496081.5:n.180A>T | ||
| NM_002116.7:c.363A>T | NP_002107.3:p.Ile121= | |
| NM_002116.8:c.363A>T MANE Select | NP_002107.3:p.Ile121= |