Linked Data
gnomAD v4:
12-121133081-C-A
COSMIC:
COSM935994
MyVariant Identifiers:
chr12:g.121570884C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121133081C>A , CM000674.2:g.121133081C>A | GRCh38 |
| NC_000012.11:g.121570884C>A , CM000674.1:g.121570884C>A | GRCh37 |
| NC_000012.10:g.120055267C>A | NCBI36 |
| NG_011471.2:g.5207C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328963.10:c.111C>A MANE Select | ENSP00000330696.6:p.Ile37= | |
| ENST00000261826.10:c.111C>A | ENSP00000261826.6:p.Ile37= | |
| ENST00000328963.9:c.111C>A | ENSP00000330696.6:p.Ile37= | |
| ENST00000535250.5:c.111C>A | ENSP00000442572.2:p.Ile37= | |
| ENST00000535600.2:c.111C>A | ENSP00000442470.1:p.Ile37= | |
| ENST00000535928.5:c.111C>A | ENSP00000439961.1:p.Ile37= | |
| ENST00000537312.5:c.111C>A | ENSP00000438586.1:p.Ile37= | |
| ENST00000538011.5:c.111C>A | ENSP00000439247.1:p.Ile37= | |
| ENST00000539606.5:c.111C>A | ENSP00000445325.1:p.Ile37= | |
| ENST00000539695.5:n.180C>A | ||
| ENST00000541022.5:c.111C>A | ENSP00000441230.1:p.Ile37= | |
| ENST00000541564.5:c.111C>A | ENSP00000443640.1:p.Ile37= | |
| ENST00000541716.5:c.111C>A | ENSP00000437729.1:p.Ile37= | |
| ENST00000545434.5:c.111C>A | ENSP00000445564.1:p.Ile37= | |
| NM_002562.5:c.111C>A | NP_002553.3:p.Ile37= | |
| NR_033948.1:n.254C>A | ||
| NR_033949.1:n.254C>A | ||
| NR_033950.1:n.254C>A | ||
| NR_033951.1:n.254C>A | ||
| NR_033952.1:n.254C>A | ||
| NR_033953.1:n.263C>A | ||
| NR_033954.1:n.254C>A | ||
| NR_033955.1:n.254C>A | ||
| NR_033956.1:n.254C>A | ||
| XM_011538418.1:c.111C>A | XP_011536720.1:p.Ile37= | |
| XM_011538419.1:c.-33C>A | XP_011536721.1:n.-33C>A | |
| XM_011538420.1:c.-451C>A | XP_011536722.1:n.-451C>A | |
| XM_011538419.3:c.-33C>A | XP_011536721.1:n.-33C>A | |
| XM_011538420.3:c.-451C>A | XP_011536722.1:n.-451C>A | |
| XM_017019364.2:c.-403C>A | XP_016874853.1:n.-403C>A | |
| XM_017019365.2:c.-234C>A | XP_016874854.1:n.-234C>A | |
| XM_017019366.2:c.-570C>A | XP_016874855.1:n.-570C>A | |
| XM_017019367.2:c.-401C>A | XP_016874856.1:n.-401C>A | |
| XR_001749352.2:n.187-6240G>T | ||
| XR_001749354.2:n.187-6240G>T | ||
| NM_002562.6:c.111C>A MANE Select | NP_002553.3:p.Ile37= | |
| NR_033948.2:n.206C>A | ||
| NR_033949.2:n.206C>A | ||
| NR_033950.2:n.206C>A | ||
| NR_033951.2:n.206C>A | ||
| NR_033952.2:n.206C>A | ||
| NR_033953.2:n.206C>A | ||
| NR_033954.2:n.206C>A | ||
| NR_033955.2:n.206C>A | ||
| NR_033956.2:n.206C>A |