Linked Data
MyVariant Identifiers:
chr2:g.38298246G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38071103G>A , CM000664.2:g.38071103G>A | GRCh38 |
| NC_000002.11:g.38298246G>A , CM000664.1:g.38298246G>A | GRCh37 |
| NC_000002.10:g.38151750G>A | NCBI36 |
| NG_008386.2:g.9999C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000490576.2:c.1251C>T | ENSP00000478839.2:p.Asp417= | |
| ENST00000610745.5:c.1251C>T MANE Select | ENSP00000478561.1:p.Asp417= | |
| ENST00000492443.1:n.629C>T | ||
| ENST00000494864.1:c.138C>T | ENSP00000479876.1:p.Asp46= | |
| ENST00000610745.4:c.1251C>T | ENSP00000478561.1:p.Asp417= | |
| ENST00000614273.1:c.1251C>T | ENSP00000483678.1:p.Asp417= | |
| NM_000104.3:c.1251C>T | NP_000095.2:p.Asp417= | |
| NM_000104.4:c.1251C>T MANE Select | NP_000095.2:p.Asp417= |