Linked Data
ClinVar Variation Id:
828677
dbSNP Id:
rs756800740
ExAC:
7:87179517 C / T
gnomAD v2:
7-87179517-C-T
gnomAD v4:
7-87550201-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87550201C>T , CM000669.2:g.87550201C>T | GRCh38 |
| NC_000007.13:g.87179517C>T , CM000669.1:g.87179517C>T | GRCh37 |
| NC_000007.12:g.87017453C>T | NCBI36 |
| NG_011513.1:g.168048G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265724.8:c.1320G>A | ENSP00000265724.3:p.Met440Ile | |
| ENST00000622132.5:c.1320G>A MANE Select | ENSP00000478255.1:p.Met440Ile | |
| ENST00000265724.7:c.1320G>A | ENSP00000265724.3:p.Met440Ile | |
| ENST00000543898.5:c.1128G>A | ENSP00000444095.1:p.Met376Ile | |
| ENST00000622132.4:c.1320G>A | ENSP00000478255.1:p.Met440Ile | |
| NM_000927.4:c.1320G>A | NP_000918.2:p.Met440Ile | |
| NM_001348944.1:c.1320G>A | NP_001335873.1:p.Met440Ile | |
| NM_001348945.1:c.1530G>A | NP_001335874.1:p.Met510Ile | |
| NM_001348946.1:c.1320G>A | NP_001335875.1:p.Met440Ile | |
| NM_001348946.2:c.1320G>A MANE Select | NP_001335875.1:p.Met440Ile | |
| NM_000927.5:c.1320G>A | NP_000918.2:p.Met440Ile | |
| NM_001348944.2:c.1320G>A | NP_001335873.1:p.Met440Ile | |
| NM_001348945.2:c.1530G>A | NP_001335874.1:p.Met510Ile |