Linked Data
MyVariant Identifiers:
chr7:g.146829597C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132505C>A , CM000669.2:g.147132505C>A | GRCh38 |
| NC_000007.13:g.146829597C>A , CM000669.1:g.146829597C>A | GRCh37 |
| NC_000007.12:g.146460530C>A | NCBI36 |
| NG_007092.2:g.1021145C>A | |
| NG_007092.3:g.1021505C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1344C>A MANE Select | ENSP00000354778.3:p.Ser448= | |
| ENST00000636561.1:n.1247C>A | ||
| ENST00000636870.1:n.1206C>A | ||
| ENST00000637150.1:n.1273C>A | ||
| ENST00000637694.1:n.1247C>A | ||
| ENST00000637825.1:n.827C>A | ||
| ENST00000638117.1:n.1247C>A | ||
| ENST00000361727.7:c.1344C>A | ENSP00000354778.3:p.Ser448= | |
| NM_014141.5:c.1344C>A | NP_054860.1:p.Ser448= | |
| XM_017011950.2:c.1344C>A | XP_016867439.1:p.Ser448= | |
| NM_014141.6:c.1344C>A MANE Select | NP_054860.1:p.Ser448= |