Linked Data
MyVariant Identifiers:
chr1:g.152283765T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152311289T>G , CM000663.2:g.152311289T>G | GRCh38 |
| NC_000001.10:g.152283765T>G , CM000663.1:g.152283765T>G | GRCh37 |
| NC_000001.9:g.150550389T>G | NCBI36 |
| NG_016190.1:g.18915A>C , LRG_1028:g.18915A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.3597A>C MANE Select | ENSP00000357789.1:p.Thr1199= | |
| ENST00000368799.1:c.3597A>C | ENSP00000357789.1:p.Thr1199= | |
| NM_002016.1:c.3597A>C , LRG_1028t1:c.3597A>C | NP_002007.1:p.Thr1199= | |
| XM_011509329.1:c.3597A>C | XP_011507631.1:p.Thr1199= | |
| NM_002016.2:c.3597A>C MANE Select | NP_002007.1:p.Thr1199= |