Linked Data
ClinVar Variation Id:
2853172
ClinVar RCV Id:
RCV003613383
MyVariant Identifiers:
chr6:g.51524712G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.51659914G>A , CM000668.2:g.51659914G>A | GRCh38 |
| NC_000006.11:g.51524712G>A , CM000668.1:g.51524712G>A | GRCh37 |
| NC_000006.10:g.51632671G>A | NCBI36 |
| NG_008753.1:g.432712C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371117.8:c.10212C>T MANE Select | ENSP00000360158.3:p.Ile3404= | |
| ENST00000371117.7:c.10212C>T | ENSP00000360158.3:p.Ile3404= | |
| NM_138694.3:c.10212C>T | NP_619639.3:p.Ile3404= | |
| XM_011514679.1:c.10212C>T | XP_011512981.1:p.Ile3404= | |
| XM_011514680.1:c.10212C>T | XP_011512982.1:p.Ile3404= | |
| XM_011514681.1:c.10083C>T | XP_011512983.1:p.Ile3361= | |
| XM_011514682.1:c.10074C>T | XP_011512984.1:p.Ile3358= | |
| XM_011514683.1:c.9570C>T | XP_011512985.1:p.Ile3190= | |
| XM_011514684.1:c.9501C>T | XP_011512986.1:p.Ile3167= | |
| XM_011514687.1:c.10157-10694C>T | XP_011512989.1:n.10157-10694C>T | |
| XM_011514690.1:c.4287C>T | XP_011512992.1:p.Ile1429= | |
| XM_011514691.1:c.4287C>T | XP_011512993.1:p.Ile1429= | |
| XR_926870.1:n.535+7541G>A | ||
| XR_926871.1:n.403+7541G>A | ||
| XR_926872.1:n.535+7541G>A | ||
| XM_011514680.3:c.10212C>T | XP_011512982.1:p.Ile3404= | |
| XM_011514682.3:c.10074C>T | XP_011512984.1:p.Ile3358= | |
| XM_011514683.3:c.9570C>T | XP_011512985.1:p.Ile3190= | |
| XM_011514684.3:c.9501C>T | XP_011512986.1:p.Ile3167= | |
| XM_011514690.3:c.4287C>T | XP_011512992.1:p.Ile1429= | |
| XM_011514691.3:c.4287C>T | XP_011512993.1:p.Ile1429= | |
| XM_017010944.2:c.10212C>T | XP_016866433.1:p.Ile3404= | |
| XM_017010945.2:c.10137C>T | XP_016866434.1:p.Ile3379= | |
| XM_017010946.2:c.10017C>T | XP_016866435.1:p.Ile3339= | |
| XM_017010947.2:c.9948C>T | XP_016866436.1:p.Ile3316= | |
| XM_017010948.2:c.9501C>T | XP_016866437.1:p.Ile3167= | |
| XM_017010949.2:c.8352C>T | XP_016866438.1:p.Ile2784= | |
| XR_001743469.1:n.10488C>T | ||
| XR_001744157.1:n.3145+7541G>A | ||
| XR_926870.2:n.3145+7541G>A | ||
| XR_926871.2:n.3013+7541G>A | ||
| XR_926872.2:n.3145+7541G>A | ||
| NM_138694.4:c.10212C>T MANE Select | NP_619639.3:p.Ile3404= |