Linked Data
MyVariant Identifiers:
chr19:g.55665437C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154069C>T , CM000681.2:g.55154069C>T | GRCh38 |
| NC_000019.9:g.55665437C>T , CM000681.1:g.55665437C>T | GRCh37 |
| NC_000019.8:g.60357249C>T | NCBI36 |
| NG_007866.2:g.8664G>A , LRG_432:g.8664G>A | |
| NG_011829.2:g.170G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.510G>A MANE Select | ENSP00000341838.5:p.Arg170= | |
| ENST00000665070.1:c.543G>A | ENSP00000499482.1:p.Arg181= | |
| ENST00000344887.9:c.510G>A | ENSP00000341838.5:p.Arg170= | |
| ENST00000585806.5:n.509G>A | ||
| ENST00000588882.1:c.435G>A | ENSP00000466729.1:p.Arg145= | |
| ENST00000589864.1:n.338G>A | ||
| NM_000363.4:c.510G>A , LRG_432t1:c.510G>A | NP_000354.4:p.Arg170= | |
| NM_000363.5:c.510G>A MANE Select | NP_000354.4:p.Arg170= |