Linked Data
MyVariant Identifiers:
chr6:g.6224953G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.6224720G>T , CM000668.2:g.6224720G>T | GRCh38 |
| NC_000006.11:g.6224953G>T , CM000668.1:g.6224953G>T | GRCh37 |
| NC_000006.10:g.6169952G>T | NCBI36 |
| NG_008107.1:g.100972C>A , LRG_549:g.100972C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264870.8:c.939C>A MANE Select | ENSP00000264870.3:p.Gly313= | |
| ENST00000264870.7:c.939C>A | ENSP00000264870.3:p.Gly313= | |
| ENST00000445223.1:c.89C>A | ||
| NM_000129.3:c.939C>A , LRG_549t1:c.939C>A | NP_000120.2:p.Gly313= | |
| XM_006715010.2:c.939C>A | XP_006715073.1:p.Gly313= | |
| XM_011514342.1:c.1101C>A | XP_011512644.1:p.Gly367= | |
| NM_000129.4:c.939C>A MANE Select | NP_000120.2:p.Gly313= |