Linked Data
MyVariant Identifiers:
chr6:g.18143902T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18143671T>C , CM000668.2:g.18143671T>C | GRCh38 |
| NC_000006.11:g.18143902T>C , CM000668.1:g.18143902T>C | GRCh37 |
| NC_000006.10:g.18251881T>C | NCBI36 |
| NG_012137.2:g.16473A>G | |
| NG_012137.3:g.16473A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000309983.5:c.291A>G MANE Select | ENSP00000312304.4:p.Gln97= | |
| ENST00000309983.4:c.291A>G | ENSP00000312304.4:p.Gln97= | |
| NM_000367.3:c.291A>G | NP_000358.1:p.Gln97= | |
| XM_011514839.1:c.291A>G | XP_011513141.1:p.Gln97= | |
| XM_011514840.1:c.222A>G | XP_011513142.1:p.Gln74= | |
| NM_000367.4:c.291A>G | NP_000358.1:p.Gln97= | |
| NM_001346817.1:c.291A>G | NP_001333746.1:p.Gln97= | |
| NM_001346818.1:c.291A>G | NP_001333747.1:p.Gln97= | |
| NM_000367.5:c.291A>G MANE Select | NP_000358.1:p.Gln97= |