Linked Data
MyVariant Identifiers:
chr7:g.5642901T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5603270T>G , CM000669.2:g.5603270T>G | GRCh38 |
| NC_000007.13:g.5642901T>G , CM000669.1:g.5642901T>G | GRCh37 |
| NC_000007.12:g.5609427T>G | NCBI36 |
| NG_030004.1:g.15466T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382361.8:c.846T>G MANE Select | ENSP00000371798.3:p.Ser282= | |
| ENST00000382361.7:c.846T>G | ENSP00000371798.3:p.Ser282= | |
| ENST00000405801.2:c.12T>G | ENSP00000383982.2:p.Ser4= | |
| ENST00000444748.5:c.12T>G | ENSP00000404506.1:p.Ser4= | |
| ENST00000447103.5:c.12T>G | ENSP00000409967.1:p.Ser4= | |
| ENST00000473330.1:n.399T>G | ||
| NM_003088.3:c.846T>G | NP_003079.1:p.Ser282= | |
| NM_003088.4:c.846T>G MANE Select | NP_003079.1:p.Ser282= |