Linked Data
MyVariant Identifiers:
chr2:g.38298336T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071193T>C , CM000664.2:g.38071193T>C | GRCh38 |
| NC_000002.11:g.38298336T>C , CM000664.1:g.38298336T>C | GRCh37 |
| NC_000002.10:g.38151840T>C | NCBI36 |
| NG_008386.2:g.9909A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.1161A>G | ENSP00000478839.2:p.Glu387= | |
| ENST00000610745.5:c.1161A>G MANE Select | ENSP00000478561.1:p.Glu387= | |
| ENST00000492443.1:n.539A>G | ||
| ENST00000494864.1:c.48A>G | ENSP00000479876.1:p.Glu16= | |
| ENST00000610745.4:c.1161A>G | ENSP00000478561.1:p.Glu387= | |
| ENST00000613082.1:n.556A>G | ||
| ENST00000614273.1:c.1161A>G | ENSP00000483678.1:p.Glu387= | |
| NM_000104.3:c.1161A>G | NP_000095.2:p.Glu387= | |
| NM_000104.4:c.1161A>G MANE Select | NP_000095.2:p.Glu387= |