Linked Data
dbSNP Id:
rs777571791
ExAC:
16:89341539 C / A
gnomAD v2:
16-89341539-C-A
gnomAD v4:
16-89275131-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89275131C>A , CM000678.2:g.89275131C>A | GRCh38 |
| NC_000016.9:g.89341539C>A , CM000678.1:g.89341539C>A | GRCh37 |
| NC_000016.8:g.87869040C>A | NCBI36 |
| NG_032003.1:g.220431G>T | |
| NG_032003.2:g.220431G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301030.10:c.7531G>T MANE Select | ENSP00000301030.4:p.Val2511Phe | |
| ENST00000330736.10:c.*7334G>T | ENSP00000330815.5:n.*7334G>T | |
| ENST00000378330.7:c.7531G>T | ENSP00000367581.2:p.Val2511Phe | |
| ENST00000642600.1:c.7531G>T | ENSP00000495226.1:p.Val2511Phe | |
| ENST00000644285.1:c.805G>T | ENSP00000496476.1:p.Val269Phe | |
| ENST00000301030.8:c.7531G>T | ENSP00000301030.4:p.Val2511Phe | |
| ENST00000330736.9:c.*7334G>T | ENSP00000330815.5:n.*7334G>T | |
| ENST00000378330.6:c.7531G>T | ENSP00000367581.2:p.Val2511Phe | |
| ENST00000562194.1:c.212G>T | ||
| NM_001256182.1:c.7531G>T | NP_001243111.1:p.Val2511Phe | |
| NM_001256183.1:c.7531G>T | NP_001243112.1:p.Val2511Phe | |
| NM_013275.5:c.7531G>T | NP_037407.4:p.Val2511Phe | |
| XM_006721181.1:c.7429G>T | XP_006721244.1:p.Val2477Phe | |
| XM_006721184.2:c.7234G>T | XP_006721247.1:p.Val2412Phe | |
| XM_011523051.1:c.7531G>T | XP_011521353.1:p.Val2511Phe | |
| XM_011523052.1:c.7531G>T | XP_011521354.1:p.Val2511Phe | |
| XM_011523053.1:c.7531G>T | XP_011521355.1:p.Val2511Phe | |
| XM_011523054.1:c.7429G>T | XP_011521356.1:p.Val2477Phe | |
| XM_011523055.1:c.7429G>T | XP_011521357.1:p.Val2477Phe | |
| XM_011523056.1:c.7402G>T | XP_011521358.1:p.Val2468Phe | |
| XM_011523057.1:c.7531G>T | XP_011521359.1:p.Val2511Phe | |
| XM_011523051.3:c.7531G>T | XP_011521353.1:p.Val2511Phe | |
| XM_011523053.2:c.7531G>T | XP_011521355.1:p.Val2511Phe | |
| XM_011523054.2:c.7429G>T | XP_011521356.1:p.Val2477Phe | |
| XM_011523055.2:c.7429G>T | XP_011521357.1:p.Val2477Phe | |
| XM_011523056.2:c.7402G>T | XP_011521358.1:p.Val2468Phe | |
| XM_011523057.2:c.7531G>T | XP_011521359.1:p.Val2511Phe | |
| XM_017023182.2:c.7531G>T | XP_016878671.1:p.Val2511Phe | |
| XM_017023183.1:c.7531G>T | XP_016878672.1:p.Val2511Phe | |
| XM_017023184.1:c.7531G>T | XP_016878673.1:p.Val2511Phe | |
| XM_017023185.1:c.7531G>T | XP_016878674.1:p.Val2511Phe | |
| XM_017023186.1:c.7531G>T | XP_016878675.1:p.Val2511Phe | |
| XM_017023187.1:c.7531G>T | XP_016878676.1:p.Val2511Phe | |
| XM_024450244.1:c.7429G>T | XP_024306012.1:p.Val2477Phe | |
| NM_013275.6:c.7531G>T MANE Select | NP_037407.4:p.Val2511Phe | |
| NM_001256182.2:c.7531G>T | NP_001243111.1:p.Val2511Phe | |
| NM_001256183.2:c.7531G>T | NP_001243112.1:p.Val2511Phe |