Linked Data
MyVariant Identifiers:
chr2:g.189923617A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189058891A>G , CM000664.2:g.189058891A>G | GRCh38 |
| NC_000002.11:g.189923617A>G , CM000664.1:g.189923617A>G | GRCh37 |
| NC_000002.10:g.189631862A>G | NCBI36 |
| NG_011799.1:g.125989T>C | |
| NG_011799.2:g.125989T>C | |
| NG_011799.3:g.171411T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374866.9:c.2088T>C MANE Select | ENSP00000364000.3:p.Gly696= | |
| ENST00000374866.7:c.2088T>C | ENSP00000364000.3:p.Gly696= | |
| ENST00000470524.2:n.194T>C | ||
| ENST00000618828.1:c.927T>C | ENSP00000482184.1:p.Gly309= | |
| NM_000393.3:c.2088T>C | NP_000384.2:p.Gly696= | |
| XM_011510573.1:c.1950T>C | XP_011508875.1:p.Gly650= | |
| NM_000393.4:c.2088T>C | NP_000384.2:p.Gly696= | |
| XM_011510573.3:c.1950T>C | XP_011508875.1:p.Gly650= | |
| NM_000393.5:c.2088T>C MANE Select | NP_000384.2:p.Gly696= |