Linked Data
MyVariant Identifiers:
chr1:g.152283456T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152310980T>C , CM000663.2:g.152310980T>C | GRCh38 |
| NC_000001.10:g.152283456T>C , CM000663.1:g.152283456T>C | GRCh37 |
| NC_000001.9:g.150550080T>C | NCBI36 |
| NG_016190.1:g.19224A>G , LRG_1028:g.19224A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.3906A>G MANE Select | ENSP00000357789.1:p.Ser1302= | |
| ENST00000368799.1:c.3906A>G | ENSP00000357789.1:p.Ser1302= | |
| NM_002016.1:c.3906A>G , LRG_1028t1:c.3906A>G | NP_002007.1:p.Ser1302= | |
| XM_011509329.1:c.3906A>G | XP_011507631.1:p.Ser1302= | |
| NM_002016.2:c.3906A>G MANE Select | NP_002007.1:p.Ser1302= |