Linked Data
MyVariant Identifiers:
chr17:g.42449759C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372391C>T , CM000679.2:g.44372391C>T | GRCh38 |
| NC_000017.10:g.42449759C>T , CM000679.1:g.42449759C>T | GRCh37 |
| NC_000017.9:g.39805285C>T | NCBI36 |
| NG_008331.1:g.22115G>A , LRG_479:g.22115G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3093G>A MANE Select | ENSP00000262407.5:p.Leu1031= | |
| ENST00000648408.1:c.2407G>A | ||
| ENST00000262407.5:c.3093G>A | ENSP00000262407.5:p.Leu1031= | |
| ENST00000587295.5:c.286G>A | ||
| ENST00000588098.1:c.70G>A | ||
| NM_000419.3:c.3093G>A , LRG_479t1:c.3093G>A | NP_000410.2:p.Leu1031= | |
| XM_011524749.1:c.2991G>A | XP_011523051.1:p.Leu997= | |
| XM_011524750.1:c.2976G>A | XP_011523052.1:p.Leu992= | |
| NM_000419.4:c.3093G>A | NP_000410.2:p.Leu1031= | |
| NM_000419.5:c.3093G>A MANE Select | NP_000410.2:p.Leu1031= |