Linked Data
MyVariant Identifiers:
chr2:g.190428791C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.189564065C>G , CM000664.2:g.189564065C>G | GRCh38 |
| NC_000002.11:g.190428791C>G , CM000664.1:g.190428791C>G | GRCh37 |
| NC_000002.10:g.190137036C>G | NCBI36 |
| NG_009027.1:g.21747G>C , LRG_837:g.21747G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261024.7:c.921G>C MANE Select | ENSP00000261024.3:p.Val307= | |
| ENST00000261024.6:c.921G>C | ENSP00000261024.2:p.Val307= | |
| NM_014585.5:c.921G>C , LRG_837t1:c.921G>C | NP_055400.1:p.Val307= | |
| XM_005246505.1:c.801G>C | XP_005246562.1:p.Val267= | |
| XM_005246505.2:c.801G>C | XP_005246562.1:p.Val267= | |
| XM_017003938.2:c.801G>C | XP_016859427.1:p.Val267= | |
| NM_014585.6:c.921G>C MANE Select | NP_055400.1:p.Val307= |