Linked Data
MyVariant Identifiers:
chr2:g.45169330G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.44942191G>T , CM000664.2:g.44942191G>T | GRCh38 |
| NC_000002.11:g.45169330G>T , CM000664.1:g.45169330G>T | GRCh37 |
| NC_000002.10:g.45022834G>T | NCBI36 |
| NG_016222.1:g.5294G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260653.5:c.87G>T MANE Select | ENSP00000260653.3:p.Leu29= | |
| ENST00000260653.4:c.87G>T | ENSP00000260653.3:p.Leu29= | |
| NM_005413.3:c.87G>T | NP_005404.1:p.Leu29= | |
| XM_011533042.1:c.87G>T | XP_011531344.1:p.Leu29= | |
| NM_005413.4:c.87G>T MANE Select | NP_005404.1:p.Leu29= |