Linked Data
MyVariant Identifiers:
chr4:g.41747917C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.41745900C>A , CM000666.2:g.41745900C>A | GRCh38 |
| NC_000004.11:g.41747917C>A , CM000666.1:g.41747917C>A | GRCh37 |
| NC_000004.10:g.41442674C>A | NCBI36 |
| NG_008243.1:g.8071G>T , LRG_513:g.8071G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226382.4:c.852G>T MANE Select | ENSP00000226382.2:p.Pro284= | |
| ENST00000226382.3:c.852G>T | ENSP00000226382.2:p.Pro284= | |
| NM_003924.3:c.852G>T , LRG_513t1:c.852G>T | NP_003915.2:p.Pro284= | |
| NM_003924.4:c.852G>T MANE Select | NP_003915.2:p.Pro284= |