Linked Data
MyVariant Identifiers:
chr1:g.35227020C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34761419C>G , CM000663.2:g.34761419C>G | GRCh38 |
| NC_000001.10:g.35227020C>G , CM000663.1:g.35227020C>G | GRCh37 |
| NC_000001.9:g.34999607C>G | NCBI36 |
| NG_016243.1:g.6679C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000339480.3:c.165C>G (GJB4) MANE Select | ENSP00000345868.1:p.Thr55= | |
| ENST00000339480.1:c.165C>G (GJB4) | ENSP00000345868.1:p.Thr55= | |
| ENST00000426886.1:c.208-43010G>C (SMIM12) | ENSP00000429902.1:n.208-43010G>C | |
| NM_153212.2:c.165C>G (GJB4) | NP_694944.1:p.Thr55= | |
| XM_011540679.1:c.165C>G (GJB4) | XP_011538981.1:p.Thr55= | |
| XR_947179.1:n.1002-17970G>C | ||
| XM_011540679.2:c.165C>G (GJB4) | XP_011538981.1:p.Thr55= | |
| XR_001737967.1:n.1023+36952G>C | ||
| NM_153212.3:c.165C>G (GJB4) MANE Select | NP_694944.1:p.Thr55= |