Linked Data
MyVariant Identifiers:
chr7:g.146829438C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132346C>T , CM000669.2:g.147132346C>T | GRCh38 |
| NC_000007.13:g.146829438C>T , CM000669.1:g.146829438C>T | GRCh37 |
| NC_000007.12:g.146460371C>T | NCBI36 |
| NG_007092.2:g.1020986C>T | |
| NG_007092.3:g.1021346C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1185C>T MANE Select | ENSP00000354778.3:p.Phe395= | |
| ENST00000636561.1:n.1088C>T | ||
| ENST00000636870.1:n.1047C>T | ||
| ENST00000637150.1:n.1114C>T | ||
| ENST00000637694.1:n.1088C>T | ||
| ENST00000637825.1:n.668C>T | ||
| ENST00000638117.1:n.1088C>T | ||
| ENST00000361727.7:c.1185C>T | ENSP00000354778.3:p.Phe395= | |
| NM_014141.5:c.1185C>T | NP_054860.1:p.Phe395= | |
| XM_017011950.2:c.1185C>T | XP_016867439.1:p.Phe395= | |
| NM_014141.6:c.1185C>T MANE Select | NP_054860.1:p.Phe395= |