Linked Data
gnomAD v4:
4-41746065-G-A
COSMIC:
COSM4894239
MyVariant Identifiers:
chr4:g.41748082G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.41746065G>A , CM000666.2:g.41746065G>A | GRCh38 |
| NC_000004.11:g.41748082G>A , CM000666.1:g.41748082G>A | GRCh37 |
| NC_000004.10:g.41442839G>A | NCBI36 |
| NG_008243.1:g.7906C>T , LRG_513:g.7906C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226382.4:c.687C>T MANE Select | ENSP00000226382.2:p.Pro229= | |
| ENST00000226382.3:c.687C>T | ENSP00000226382.2:p.Pro229= | |
| ENST00000510424.2:n.508C>T | ||
| NM_003924.3:c.687C>T , LRG_513t1:c.687C>T | NP_003915.2:p.Pro229= | |
| NM_003924.4:c.687C>T MANE Select | NP_003915.2:p.Pro229= |