Linked Data
gnomAD v4:
2-232484863-G-T
COSMIC:
COSM5676158
MyVariant Identifiers:
chr2:g.233349573G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232484863G>T , CM000664.2:g.232484863G>T | GRCh38 |
| NC_000002.11:g.233349573G>T , CM000664.1:g.233349573G>T | GRCh37 |
| NC_000002.10:g.233057817G>T | NCBI36 |
| NG_034065.1:g.7997C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304546.6:c.997C>A MANE Select | ENSP00000302051.1:p.Arg333= | |
| ENST00000304546.5:c.997C>A | ENSP00000302051.1:p.Arg333= | |
| ENST00000409941.1:c.997C>A | ENSP00000386333.1:p.Arg333= | |
| ENST00000482346.1:n.1308C>A | ||
| NM_001290787.1:c.997C>A | NP_001277716.1:p.Arg333= | |
| NM_004826.3:c.997C>A | NP_004817.2:p.Arg333= | |
| NM_004826.4:c.997C>A MANE Select | NP_004817.2:p.Arg333= | |
| NM_001290787.2:c.997C>A | NP_001277716.1:p.Arg333= |