Linked Data
ClinVar Variation Id:
1047081
dbSNP Id:
rs1428042303
gnomAD v2:
11-111959632-G-T
gnomAD v4:
11-112088908-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112088908G>T , CM000673.2:g.112088908G>T | GRCh38 |
| NC_000011.9:g.111959632G>T , CM000673.1:g.111959632G>T | GRCh37 |
| NC_000011.8:g.111464842G>T | NCBI36 |
| NG_012337.2:g.7062G>T | |
| NG_033145.1:g.2891C>A | |
| NG_012337.3:g.7062G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530923.6:c.211G>T | ENSP00000432946.2:p.Val71Phe | |
| ENST00000534010.2:c.211G>T | ENSP00000433202.2:p.Val71Phe | |
| ENST00000375549.8:c.211G>T MANE Select | ENSP00000364699.3:p.Val71Phe | |
| ENST00000528021.6:c.211G>T | ENSP00000432465.1:p.Val71Phe | |
| ENST00000640554.1:c.*283G>T | ENSP00000491141.1:n.*283G>T | |
| ENST00000375549.7:c.211G>T | ENSP00000364699.3:p.Val71Phe | |
| ENST00000525291.5:c.94G>T | ENSP00000436669.1:p.Val32Phe | |
| ENST00000525987.5:n.216G>T | ||
| ENST00000526592.5:c.211G>T | ENSP00000432005.1:p.Val71Phe | |
| ENST00000528021.5:c.211G>T | ENSP00000432465.1:p.Val71Phe | |
| ENST00000528048.5:c.169+935G>T | ENSP00000436217.1:n.169+935G>T | |
| ENST00000528182.5:c.211G>T | ENSP00000435475.1:p.Val71Phe | |
| ENST00000530923.5:c.201G>T | ||
| ENST00000531744.5:c.211G>T | ENSP00000456957.1:p.Val71Phe | |
| ENST00000532699.1:c.211G>T | ENSP00000456434.1:p.Val71Phe | |
| ENST00000534010.1:c.42G>T | ||
| ENST00000614349.4:c.211G>T | ENSP00000480666.1:p.Val71Phe | |
| NM_001276503.1:c.169+935G>T | NP_001263432.1:n.169+935G>T | |
| NM_001276504.1:c.94G>T | NP_001263433.1:p.Val32Phe | |
| NM_001276506.1:c.211G>T | NP_001263435.1:p.Val71Phe | |
| NM_003002.3:c.211G>T | NP_002993.1:p.Val71Phe | |
| NR_077060.1:n.295G>T | ||
| NM_003002.4:c.211G>T MANE Select | NP_002993.1:p.Val71Phe | |
| NM_001276503.2:c.169+935G>T | NP_001263432.1:n.169+935G>T | |
| NM_001276504.2:c.94G>T | NP_001263433.1:p.Val32Phe | |
| NM_001276506.2:c.211G>T | NP_001263435.1:p.Val71Phe | |
| NR_077060.2:n.246G>T |