Linked Data
ClinVar Variation Id:
454816
ClinVar RCV Id:
RCV000531192
dbSNP Id:
rs113742238
ExAC:
5:13776691 C / T
gnomAD v2:
5-13776691-C-T
gnomAD v3:
5-13776582-C-T
gnomAD v4:
5-13776582-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13776582C>T , CM000667.2:g.13776582C>T | GRCh38 |
| NC_000005.9:g.13776691C>T , CM000667.1:g.13776691C>T | GRCh37 |
| NC_000005.8:g.13829691C>T | NCBI36 |
| NG_013081.1:g.172899G>A | |
| NG_013081.2:g.172899G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9230G>A MANE Select | ENSP00000265104.4:p.Arg3077Gln | |
| ENST00000681290.1:c.9185G>A | ENSP00000505288.1:p.Arg3062Gln | |
| ENST00000265104.4:c.9230G>A | ENSP00000265104.4:p.Arg3077Gln | |
| NM_001369.2:c.9230G>A | NP_001360.1:p.Arg3077Gln | |
| XM_005248262.2:c.9185G>A | XP_005248319.1:p.Arg3062Gln | |
| XM_005248262.3:c.9338G>A | XP_005248319.2:p.Arg3113Gln | |
| XM_017009177.1:c.9338G>A | XP_016864666.1:p.Arg3113Gln | |
| XM_017009178.1:c.8243G>A | XP_016864667.1:p.Arg2748Gln | |
| XM_017009179.2:c.8243G>A | XP_016864668.1:p.Arg2748Gln | |
| XM_017009180.1:c.9338G>A | XP_016864669.1:p.Arg3113Gln | |
| XM_017009181.1:c.9338G>A | XP_016864670.1:p.Arg3113Gln | |
| XM_017009182.1:c.9338G>A | XP_016864671.1:p.Arg3113Gln | |
| XM_017009183.1:c.9338G>A | XP_016864672.1:p.Arg3113Gln | |
| XM_017009185.1:c.4427G>A | XP_016864674.1:p.Arg1476Gln | |
| XM_017009186.1:c.3980G>A | XP_016864675.1:p.Arg1327Gln | |
| XM_017009188.1:c.3317G>A | XP_016864677.1:p.Arg1106Gln | |
| XM_024454388.1:c.8243G>A | XP_024310156.1:p.Arg2748Gln | |
| XM_024454389.1:c.7832G>A | XP_024310157.1:p.Arg2611Gln | |
| NM_001369.3:c.9230G>A MANE Select | NP_001360.1:p.Arg3077Gln |