Linked Data
dbSNP Id:
rs753143710
ExAC:
6:51613016 T / C
gnomAD v2:
6-51613016-T-C
gnomAD v4:
6-51748218-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51748218T>C , CM000668.2:g.51748218T>C | GRCh38 |
| NC_000006.11:g.51613016T>C , CM000668.1:g.51613016T>C | GRCh37 |
| NC_000006.10:g.51720975T>C | NCBI36 |
| NG_008753.1:g.344408A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.9398A>G MANE Select | ENSP00000360158.3:p.Tyr3133Cys | |
| ENST00000340994.4:c.9398A>G | ENSP00000341097.4:p.Tyr3133Cys | |
| ENST00000371117.7:c.9398A>G | ENSP00000360158.3:p.Tyr3133Cys | |
| NM_138694.3:c.9398A>G | NP_619639.3:p.Tyr3133Cys | |
| NM_170724.2:c.9398A>G | NP_733842.2:p.Tyr3133Cys | |
| XM_011514679.1:c.9398A>G | XP_011512981.1:p.Tyr3133Cys | |
| XM_011514680.1:c.9398A>G | XP_011512982.1:p.Tyr3133Cys | |
| XM_011514681.1:c.9269A>G | XP_011512983.1:p.Tyr3090Cys | |
| XM_011514682.1:c.9260A>G | XP_011512984.1:p.Tyr3087Cys | |
| XM_011514683.1:c.8756A>G | XP_011512985.1:p.Tyr2919Cys | |
| XM_011514684.1:c.8687A>G | XP_011512986.1:p.Tyr2896Cys | |
| XM_011514685.1:c.9398A>G | XP_011512987.1:p.Tyr3133Cys | |
| XM_011514686.1:c.9398A>G | XP_011512988.1:p.Tyr3133Cys | |
| XM_011514687.1:c.9398A>G | XP_011512989.1:p.Tyr3133Cys | |
| XM_011514688.1:c.9398A>G | XP_011512990.1:p.Tyr3133Cys | |
| XM_011514690.1:c.3473A>G | XP_011512992.1:p.Tyr1158Cys | |
| XM_011514691.1:c.3473A>G | XP_011512993.1:p.Tyr1158Cys | |
| XM_011514680.3:c.9398A>G | XP_011512982.1:p.Tyr3133Cys | |
| XM_011514682.3:c.9260A>G | XP_011512984.1:p.Tyr3087Cys | |
| XM_011514683.3:c.8756A>G | XP_011512985.1:p.Tyr2919Cys | |
| XM_011514684.3:c.8687A>G | XP_011512986.1:p.Tyr2896Cys | |
| XM_011514686.2:c.9398A>G | XP_011512988.1:p.Tyr3133Cys | |
| XM_011514688.2:c.9398A>G | XP_011512990.1:p.Tyr3133Cys | |
| XM_011514690.3:c.3473A>G | XP_011512992.1:p.Tyr1158Cys | |
| XM_011514691.3:c.3473A>G | XP_011512993.1:p.Tyr1158Cys | |
| XM_017010944.2:c.9398A>G | XP_016866433.1:p.Tyr3133Cys | |
| XM_017010945.2:c.9323A>G | XP_016866434.1:p.Tyr3108Cys | |
| XM_017010946.2:c.9203A>G | XP_016866435.1:p.Tyr3068Cys | |
| XM_017010947.2:c.9134A>G | XP_016866436.1:p.Tyr3045Cys | |
| XM_017010948.2:c.8687A>G | XP_016866437.1:p.Tyr2896Cys | |
| XM_017010949.2:c.7538A>G | XP_016866438.1:p.Tyr2513Cys | |
| XM_017010950.1:c.9398A>G | XP_016866439.1:p.Tyr3133Cys | |
| XR_001743469.1:n.9674A>G | ||
| NM_138694.4:c.9398A>G MANE Select | NP_619639.3:p.Tyr3133Cys | |
| NM_170724.3:c.9398A>G | NP_733842.2:p.Tyr3133Cys |