Linked Data
MyVariant Identifiers:
chr1:g.154543896T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571420T>G , CM000663.2:g.154571420T>G | GRCh38 |
| NC_000001.10:g.154543896T>G , CM000663.1:g.154543896T>G | GRCh37 |
| NC_000001.9:g.152810520T>G | NCBI36 |
| NG_008027.1:g.8640T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.597T>G MANE Select | ENSP00000357461.3:p.Pro199= | |
| ENST00000636034.1:c.597T>G | ENSP00000489703.1:p.Pro199= | |
| ENST00000637900.1:c.603T>G | ENSP00000490474.1:p.Pro201= | |
| ENST00000368476.3:c.597T>G | ENSP00000357461.3:p.Pro199= | |
| NM_000748.2:c.597T>G | NP_000739.1:p.Pro199= | |
| XM_017000180.2:c.87T>G | XP_016855669.1:p.Pro29= | |
| XR_001736952.2:n.849T>G | ||
| NM_000748.3:c.597T>G MANE Select | NP_000739.1:p.Pro199= |