Linked Data
MyVariant Identifiers:
chr6:g.18122328A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.18122097A>T , CM000668.2:g.18122097A>T | GRCh38 |
| NC_000006.11:g.18122328A>T , CM000668.1:g.18122328A>T | GRCh37 |
| NC_000006.10:g.18230307A>T | NCBI36 |
| NG_016750.1:g.5524T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340650.6:c.510T>A MANE Select | ENSP00000345464.3:p.Ala170= | |
| ENST00000340650.4:c.510T>A | ENSP00000345464.3:p.Ala170= | |
| NM_198586.2:c.510T>A | NP_940988.2:p.Ala170= | |
| NM_198586.3:c.510T>A MANE Select | NP_940988.2:p.Ala170= |