Linked Data
MyVariant Identifiers:
chr6:g.24174970A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24174742A>C , CM000668.2:g.24174742A>C | GRCh38 |
| NC_000006.11:g.24174970A>C , CM000668.1:g.24174970A>C | GRCh37 |
| NC_000006.10:g.24282949A>C | NCBI36 |
| NG_012829.1:g.188311T>G | |
| NG_012829.2:g.213551T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.1419T>G MANE Select | ENSP00000367715.3:p.Ala473= | |
| ENST00000378450.6:c.678T>G | ENSP00000367711.3:p.Ala226= | |
| ENST00000378454.7:c.1419T>G | ENSP00000367715.3:p.Ala473= | |
| NM_001195610.1:c.1419T>G | NP_001182539.1:p.Ala473= | |
| NM_016356.4:c.1419T>G | NP_057440.2:p.Ala473= | |
| NM_016356.5:c.1419T>G MANE Select | NP_057440.2:p.Ala473= | |
| NM_001195610.2:c.1419T>G | NP_001182539.1:p.Ala473= |