Linked Data
MyVariant Identifiers:
chr7:g.146829483G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.147132391G>C , CM000669.2:g.147132391G>C | GRCh38 |
| NC_000007.13:g.146829483G>C , CM000669.1:g.146829483G>C | GRCh37 |
| NC_000007.12:g.146460416G>C | NCBI36 |
| NG_007092.2:g.1021031G>C | |
| NG_007092.3:g.1021391G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361727.8:c.1230G>C MANE Select | ENSP00000354778.3:p.Leu410= | |
| ENST00000636561.1:n.1133G>C | ||
| ENST00000636870.1:n.1092G>C | ||
| ENST00000637150.1:n.1159G>C | ||
| ENST00000637694.1:n.1133G>C | ||
| ENST00000637825.1:n.713G>C | ||
| ENST00000638117.1:n.1133G>C | ||
| ENST00000361727.7:c.1230G>C | ENSP00000354778.3:p.Leu410= | |
| NM_014141.5:c.1230G>C | NP_054860.1:p.Leu410= | |
| XM_017011950.2:c.1230G>C | XP_016867439.1:p.Leu410= | |
| NM_014141.6:c.1230G>C MANE Select | NP_054860.1:p.Leu410= |