Linked Data
dbSNP Id:
rs1173128919
gnomAD v3:
12-40340315-T-C
gnomAD v4:
12-40340315-T-C
MyVariant Identifiers:
chr12:g.40734117T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.40340315T>C , CM000674.2:g.40340315T>C | GRCh38 |
| NC_000012.11:g.40734117T>C , CM000674.1:g.40734117T>C | GRCh37 |
| NC_000012.10:g.39020384T>C | NCBI36 |
| NG_011709.1:g.120305T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000298910.12:c.5970T>C MANE Select | ENSP00000298910.7:p.Ile1990= | |
| ENST00000679360.1:c.*4879T>C | ENSP00000505368.1:n.*4879T>C | |
| ENST00000679532.1:c.1744T>C | ||
| ENST00000680018.1:c.1415T>C | ENSP00000505347.1:n.1415T>C | |
| ENST00000680422.1:c.1615T>C | ||
| ENST00000680425.1:c.1137T>C | ENSP00000506459.1:n.1137T>C | |
| ENST00000680453.1:c.1427T>C | ||
| ENST00000680790.1:c.5715T>C | ENSP00000505335.1:p.Ile1905= | |
| ENST00000681136.1:n.1954T>C | ||
| ENST00000681696.1:c.1653T>C | ENSP00000505871.1:p.Ile551= | |
| ENST00000298910.11:c.5970T>C | ENSP00000298910.7:p.Ile1990= | |
| ENST00000430804.5:c.3266T>C | ||
| ENST00000479187.5:n.2651T>C | ||
| NM_198578.3:c.5970T>C | NP_940980.3:p.Ile1990= | |
| XM_005268629.2:c.5970T>C | XP_005268686.1:p.Ile1990= | |
| XM_011537877.1:c.5970T>C | XP_011536179.1:p.Ile1990= | |
| XM_011537878.1:c.5970T>C | XP_011536180.1:p.Ile1990= | |
| XM_011537879.1:c.4767T>C | XP_011536181.1:p.Ile1589= | |
| XM_005268629.4:c.5970T>C | XP_005268686.1:p.Ile1990= | |
| XM_011537877.3:c.5970T>C | XP_011536179.1:p.Ile1990= | |
| XM_017018787.1:c.2886T>C | XP_016874276.1:p.Ile962= | |
| XM_017018788.2:c.2232T>C | XP_016874277.1:p.Ile744= | |
| XM_024448833.1:c.4767T>C | XP_024304601.1:p.Ile1589= | |
| NM_198578.4:c.5970T>C MANE Select | NP_940980.4:p.Ile1990= |