Linked Data
ClinVar Variation Id:
188366
ClinVar RCV Id:
RCV000168403
dbSNP Id:
rs138505566
ExAC:
5:13776703 T / C
gnomAD v2:
5-13776703-T-C
gnomAD v3:
5-13776594-T-C
gnomAD v4:
5-13776594-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13776594T>C , CM000667.2:g.13776594T>C | GRCh38 |
| NC_000005.9:g.13776703T>C , CM000667.1:g.13776703T>C | GRCh37 |
| NC_000005.8:g.13829703T>C | NCBI36 |
| NG_013081.1:g.172887A>G | |
| NG_013081.2:g.172887A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265104.5:c.9218A>G MANE Select | ENSP00000265104.4:p.Tyr3073Cys | |
| ENST00000681290.1:c.9173A>G | ENSP00000505288.1:p.Tyr3058Cys | |
| ENST00000265104.4:c.9218A>G | ENSP00000265104.4:p.Tyr3073Cys | |
| NM_001369.2:c.9218A>G | NP_001360.1:p.Tyr3073Cys | |
| XM_005248262.2:c.9173A>G | XP_005248319.1:p.Tyr3058Cys | |
| XM_005248262.3:c.9326A>G | XP_005248319.2:p.Tyr3109Cys | |
| XM_017009177.1:c.9326A>G | XP_016864666.1:p.Tyr3109Cys | |
| XM_017009178.1:c.8231A>G | XP_016864667.1:p.Tyr2744Cys | |
| XM_017009179.2:c.8231A>G | XP_016864668.1:p.Tyr2744Cys | |
| XM_017009180.1:c.9326A>G | XP_016864669.1:p.Tyr3109Cys | |
| XM_017009181.1:c.9326A>G | XP_016864670.1:p.Tyr3109Cys | |
| XM_017009182.1:c.9326A>G | XP_016864671.1:p.Tyr3109Cys | |
| XM_017009183.1:c.9326A>G | XP_016864672.1:p.Tyr3109Cys | |
| XM_017009185.1:c.4415A>G | XP_016864674.1:p.Tyr1472Cys | |
| XM_017009186.1:c.3968A>G | XP_016864675.1:p.Tyr1323Cys | |
| XM_017009188.1:c.3305A>G | XP_016864677.1:p.Tyr1102Cys | |
| XM_024454388.1:c.8231A>G | XP_024310156.1:p.Tyr2744Cys | |
| XM_024454389.1:c.7820A>G | XP_024310157.1:p.Tyr2607Cys | |
| NM_001369.3:c.9218A>G MANE Select | NP_001360.1:p.Tyr3073Cys |