Linked Data
ClinVar Variation Id:
407296
dbSNP Id:
rs113332942
ExAC:
6:38843520 C / T
gnomAD v2:
6-38843520-C-T
gnomAD v3:
6-38875744-C-T
gnomAD v4:
6-38875744-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.38875744C>T , CM000668.2:g.38875744C>T | GRCh38 |
| NC_000006.11:g.38843520C>T , CM000668.1:g.38843520C>T | GRCh37 |
| NC_000006.10:g.38951498C>T | NCBI36 |
| NG_041805.1:g.165404C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327475.11:c.7774C>T MANE Select | ENSP00000333363.7:p.Arg2592Trp | |
| ENST00000327475.10:c.7774C>T | ENSP00000333363.7:p.Arg2592Trp | |
| ENST00000359357.7:c.7123C>T | ENSP00000352312.3:p.Arg2375Trp | |
| ENST00000449981.6:c.7774C>T | ENSP00000415331.2:p.Arg2592Trp | |
| NM_001206927.1:c.7774C>T | NP_001193856.1:p.Arg2592Trp | |
| XM_011514318.1:c.7711C>T | XP_011512620.1:p.Arg2571Trp | |
| XM_011514319.1:c.7666C>T | XP_011512621.1:p.Arg2556Trp | |
| XM_011514320.1:c.7537C>T | XP_011512622.1:p.Arg2513Trp | |
| XM_011514321.1:c.7123C>T | XP_011512623.1:p.Arg2375Trp | |
| XM_011514322.1:c.7620+2368C>T | XP_011512624.1:n.7620+2368C>T | |
| XR_926078.1:n.7891C>T | ||
| NM_001371.3:c.7123C>T | NP_001362.2:p.Arg2375Trp | |
| XM_011514318.2:c.7711C>T | XP_011512620.1:p.Arg2571Trp | |
| XM_011514319.2:c.7666C>T | XP_011512621.1:p.Arg2556Trp | |
| XM_011514320.2:c.7537C>T | XP_011512622.1:p.Arg2513Trp | |
| XM_017010325.1:c.7774C>T | XP_016865814.1:p.Arg2592Trp | |
| XM_017010326.1:c.7774C>T | XP_016865815.1:p.Arg2592Trp | |
| XM_017010327.1:c.7774C>T | XP_016865816.1:p.Arg2592Trp | |
| XR_001743188.1:n.7741+2368C>T | ||
| XR_926078.2:n.7894C>T | ||
| NM_001206927.2:c.7774C>T MANE Select | NP_001193856.1:p.Arg2592Trp | |
| NM_001371.4:c.7123C>T | NP_001362.2:p.Arg2375Trp |