Linked Data
ClinVar Variation Id:
262416
dbSNP Id:
rs755688912
ExAC:
6:51712658 C / A
gnomAD v2:
6-51712658-C-A
gnomAD v3:
6-51847860-C-A
gnomAD v4:
6-51847860-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51847860C>A , CM000668.2:g.51847860C>A | GRCh38 |
| NC_000006.11:g.51712658C>A , CM000668.1:g.51712658C>A | GRCh37 |
| NC_000006.10:g.51820617C>A | NCBI36 |
| NG_008753.1:g.244766G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.8022G>T MANE Select | ENSP00000360158.3:p.Leu2674= | |
| ENST00000340994.4:c.8022G>T | ENSP00000341097.4:p.Leu2674= | |
| ENST00000371117.7:c.8022G>T | ENSP00000360158.3:p.Leu2674= | |
| NM_138694.3:c.8022G>T | NP_619639.3:p.Leu2674= | |
| NM_170724.2:c.8022G>T | NP_733842.2:p.Leu2674= | |
| XM_011514679.1:c.8022G>T | XP_011512981.1:p.Leu2674= | |
| XM_011514680.1:c.8022G>T | XP_011512982.1:p.Leu2674= | |
| XM_011514681.1:c.8022G>T | XP_011512983.1:p.Leu2674= | |
| XM_011514682.1:c.8022G>T | XP_011512984.1:p.Leu2674= | |
| XM_011514683.1:c.7380G>T | XP_011512985.1:p.Leu2460= | |
| XM_011514684.1:c.7311G>T | XP_011512986.1:p.Leu2437= | |
| XM_011514685.1:c.8022G>T | XP_011512987.1:p.Leu2674= | |
| XM_011514686.1:c.8022G>T | XP_011512988.1:p.Leu2674= | |
| XM_011514687.1:c.8022G>T | XP_011512989.1:p.Leu2674= | |
| XM_011514688.1:c.8022G>T | XP_011512990.1:p.Leu2674= | |
| XM_011514689.1:c.8022G>T | XP_011512991.1:p.Leu2674= | |
| XM_011514690.1:c.2097G>T | XP_011512992.1:p.Leu699= | |
| XM_011514691.1:c.2097G>T | XP_011512993.1:p.Leu699= | |
| XM_011514680.3:c.8022G>T | XP_011512982.1:p.Leu2674= | |
| XM_011514682.3:c.8022G>T | XP_011512984.1:p.Leu2674= | |
| XM_011514683.3:c.7380G>T | XP_011512985.1:p.Leu2460= | |
| XM_011514684.3:c.7311G>T | XP_011512986.1:p.Leu2437= | |
| XM_011514686.2:c.8022G>T | XP_011512988.1:p.Leu2674= | |
| XM_011514688.2:c.8022G>T | XP_011512990.1:p.Leu2674= | |
| XM_011514690.3:c.2097G>T | XP_011512992.1:p.Leu699= | |
| XM_011514691.3:c.2097G>T | XP_011512993.1:p.Leu699= | |
| XM_017010944.2:c.8022G>T | XP_016866433.1:p.Leu2674= | |
| XM_017010945.2:c.7947G>T | XP_016866434.1:p.Leu2649= | |
| XM_017010946.2:c.8022G>T | XP_016866435.1:p.Leu2674= | |
| XM_017010947.2:c.7758G>T | XP_016866436.1:p.Leu2586= | |
| XM_017010948.2:c.7311G>T | XP_016866437.1:p.Leu2437= | |
| XM_017010949.2:c.6162G>T | XP_016866438.1:p.Leu2054= | |
| XM_017010950.1:c.8022G>T | XP_016866439.1:p.Leu2674= | |
| XM_017010951.1:c.8022G>T | XP_016866440.1:p.Leu2674= | |
| XM_017010952.1:c.8022G>T | XP_016866441.1:p.Leu2674= | |
| XR_001743469.1:n.8298G>T | ||
| NM_138694.4:c.8022G>T MANE Select | NP_619639.3:p.Leu2674= | |
| NM_170724.3:c.8022G>T | NP_733842.2:p.Leu2674= |