Linked Data
dbSNP Id:
rs1324823314
gnomAD v2:
11-61161370-T-C
gnomAD v4:
11-61393898-T-C
COSMIC:
COSM1664598
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61393898T>C , CM000673.2:g.61393898T>C | GRCh38 |
| NC_000011.9:g.61161370T>C , CM000673.1:g.61161370T>C | GRCh37 |
| NC_000011.8:g.60917946T>C | NCBI36 |
| NG_032976.1:g.6539T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000334888.10:c.151T>C | ENSP00000334844.5:p.Tyr51His | |
| ENST00000544795.6:n.428T>C | ||
| ENST00000684926.1:n.167T>C | ||
| ENST00000688959.1:c.-109T>C | ENSP00000509213.1:n.-109T>C | |
| ENST00000690736.1:c.151T>C | ENSP00000508542.1:p.Tyr51His | |
| ENST00000515837.7:c.151T>C MANE Select | ENSP00000440638.1:p.Tyr51His | |
| ENST00000334888.9:c.151T>C | ENSP00000334844.5:p.Tyr51His | |
| ENST00000398979.7:c.-33T>C | ENSP00000381950.3:n.-33T>C | |
| ENST00000515837.6:c.151T>C | ENSP00000440638.1:p.Tyr51His | |
| ENST00000541473.1:n.165T>C | ||
| ENST00000544795.5:n.167T>C | ||
| NM_001173990.2:c.151T>C | NP_001167461.1:p.Tyr51His | |
| NM_001173991.2:c.151T>C | NP_001167462.1:p.Tyr51His | |
| NM_016499.5:c.-33T>C | NP_057583.2:n.-33T>C | |
| XM_005274039.3:c.-33T>C | XP_005274096.1:n.-33T>C | |
| NM_001330285.1:c.-33T>C | NP_001317214.1:n.-33T>C | |
| XM_005274039.4:c.-33T>C | XP_005274096.1:n.-33T>C | |
| NM_001173990.3:c.151T>C MANE Select | NP_001167461.1:p.Tyr51His | |
| NM_001173991.3:c.151T>C | NP_001167462.1:p.Tyr51His | |
| NM_001330285.2:c.-33T>C | NP_001317214.1:n.-33T>C | |
| NM_016499.6:c.-33T>C | NP_057583.2:n.-33T>C |