Linked Data
ClinVar Variation Id:
167473
dbSNP Id:
rs78518523
ExAC:
6:51523998 C / T
gnomAD v2:
6-51523998-C-T
gnomAD v3:
6-51659200-C-T
gnomAD v4:
6-51659200-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51659200C>T , CM000668.2:g.51659200C>T | GRCh38 |
| NC_000006.11:g.51523998C>T , CM000668.1:g.51523998C>T | GRCh37 |
| NC_000006.10:g.51631957C>T | NCBI36 |
| NG_008753.1:g.433426G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.10926G>A MANE Select | ENSP00000360158.3:p.Met3642Ile | |
| ENST00000371117.7:c.10926G>A | ENSP00000360158.3:p.Met3642Ile | |
| NM_138694.3:c.10926G>A | NP_619639.3:p.Met3642Ile | |
| XM_011514679.1:c.10926G>A | XP_011512981.1:p.Met3642Ile | |
| XM_011514680.1:c.10926G>A | XP_011512982.1:p.Met3642Ile | |
| XM_011514681.1:c.10797G>A | XP_011512983.1:p.Met3599Ile | |
| XM_011514682.1:c.10788G>A | XP_011512984.1:p.Met3596Ile | |
| XM_011514683.1:c.10284G>A | XP_011512985.1:p.Met3428Ile | |
| XM_011514684.1:c.10215G>A | XP_011512986.1:p.Met3405Ile | |
| XM_011514687.1:c.10157-9980G>A | XP_011512989.1:n.10157-9980G>A | |
| XM_011514690.1:c.5001G>A | XP_011512992.1:p.Met1667Ile | |
| XM_011514691.1:c.5001G>A | XP_011512993.1:p.Met1667Ile | |
| XR_926870.1:n.535+6827C>T | ||
| XR_926871.1:n.403+6827C>T | ||
| XR_926872.1:n.535+6827C>T | ||
| XM_011514680.3:c.10926G>A | XP_011512982.1:p.Met3642Ile | |
| XM_011514682.3:c.10788G>A | XP_011512984.1:p.Met3596Ile | |
| XM_011514683.3:c.10284G>A | XP_011512985.1:p.Met3428Ile | |
| XM_011514684.3:c.10215G>A | XP_011512986.1:p.Met3405Ile | |
| XM_011514690.3:c.5001G>A | XP_011512992.1:p.Met1667Ile | |
| XM_011514691.3:c.5001G>A | XP_011512993.1:p.Met1667Ile | |
| XM_017010944.2:c.10926G>A | XP_016866433.1:p.Met3642Ile | |
| XM_017010945.2:c.10851G>A | XP_016866434.1:p.Met3617Ile | |
| XM_017010946.2:c.10731G>A | XP_016866435.1:p.Met3577Ile | |
| XM_017010947.2:c.10662G>A | XP_016866436.1:p.Met3554Ile | |
| XM_017010948.2:c.10215G>A | XP_016866437.1:p.Met3405Ile | |
| XM_017010949.2:c.9066G>A | XP_016866438.1:p.Met3022Ile | |
| XR_001743469.1:n.11202G>A | ||
| XR_001744157.1:n.3145+6827C>T | ||
| XR_926870.2:n.3145+6827C>T | ||
| XR_926871.2:n.3013+6827C>T | ||
| XR_926872.2:n.3145+6827C>T | ||
| NM_138694.4:c.10926G>A MANE Select | NP_619639.3:p.Met3642Ile |