Linked Data
ClinVar Variation Id:
2157489
dbSNP Id:
rs1241193511
gnomAD v2:
17-44108848-G-C
gnomAD v3:
17-46031482-G-C
gnomAD v4:
17-46031482-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.46031482G>C , CM000679.2:g.46031482G>C | GRCh38 |
| NC_000017.10:g.44108848G>C , CM000679.1:g.44108848G>C | GRCh37 |
| NC_000017.9:g.41464695G>C | NCBI36 |
| NG_032784.1:g.198893C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432791.7:c.3312C>G MANE Select | ENSP00000387393.3:p.His1104Gln | |
| ENST00000572904.6:c.3312C>G | ENSP00000461484.1:p.His1104Gln | |
| ENST00000574590.6:c.3309C>G | ENSP00000461812.2:p.His1103Gln | |
| ENST00000575318.6:c.3120C>G | ENSP00000461299.1:p.His1040Gln | |
| ENST00000638275.1:c.3120C>G | ENSP00000492576.1:p.His1040Gln | |
| ENST00000648792.1:c.3180C>G | ENSP00000497628.1:p.His1060Gln | |
| ENST00000262419.10:c.3312C>G | ENSP00000262419.6:p.His1104Gln | |
| ENST00000432791.5:c.3309C>G | ENSP00000387393.2:p.His1103Gln | |
| ENST00000572218.5:n.7529C>G | ||
| ENST00000572904.5:c.3312C>G | ENSP00000461484.1:p.His1104Gln | |
| ENST00000574590.5:c.3312C>G | ENSP00000461812.1:p.His1104Gln | |
| ENST00000574963.1:n.1085C>G | ||
| ENST00000575318.5:c.3120C>G | ENSP00000461299.1:p.His1040Gln | |
| ENST00000576870.5:n.1284C>G | ||
| NM_001193465.1:c.3309C>G | NP_001180394.1:p.His1103Gln | |
| NM_001193466.1:c.3312C>G | NP_001180395.1:p.His1104Gln | |
| NM_015443.3:c.3312C>G | NP_056258.1:p.His1104Gln | |
| XM_006721823.1:c.3312C>G | XP_006721886.1:p.His1104Gln | |
| XM_006721824.2:c.3312C>G | XP_006721887.1:p.His1104Gln | |
| XM_011524628.1:c.3309C>G | XP_011522930.1:p.His1103Gln | |
| XM_011524629.1:c.3210C>G | XP_011522931.1:p.His1070Gln | |
| XM_011524630.1:c.3123C>G | XP_011522932.1:p.His1041Gln | |
| XM_011524631.1:c.3120C>G | XP_011522933.1:p.His1040Gln | |
| XM_011524632.1:c.2082C>G | XP_011522934.1:p.His694Gln | |
| XM_006721823.2:c.3312C>G | XP_006721886.1:p.His1104Gln | |
| XM_006721824.4:c.3312C>G | XP_006721887.1:p.His1104Gln | |
| XM_011524628.3:c.3309C>G | XP_011522930.1:p.His1103Gln | |
| XM_011524629.3:c.3210C>G | XP_011522931.1:p.His1070Gln | |
| XM_011524630.3:c.3123C>G | XP_011522932.1:p.His1041Gln | |
| XM_011524631.3:c.3120C>G | XP_011522933.1:p.His1040Gln | |
| XM_011524632.3:c.2082C>G | XP_011522934.1:p.His694Gln | |
| XM_017024488.2:c.3120C>G | XP_016879977.1:p.His1040Gln | |
| NM_001193466.2:c.3312C>G | NP_001180395.1:p.His1104Gln | |
| NM_015443.4:c.3312C>G MANE Select | NP_056258.1:p.His1104Gln | |
| NM_001193465.2:c.3309C>G | NP_001180394.1:p.His1103Gln | |
| NM_001379198.1:c.3312C>G | NP_001366127.1:p.His1104Gln |