Linked Data
ClinVar Variation Id:
143912
ClinVar RCV Id:
RCV000133447
dbSNP Id:
rs36079186
ExAC:
19:41512918 T / C
gnomAD v2:
19-41512918-T-C
gnomAD v3:
19-41007013-T-C
gnomAD v4:
19-41007013-T-C
PubMed:
PMID:17235330
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.41007013T>C , CM000681.2:g.41007013T>C | GRCh38 |
| NC_000019.9:g.41512918T>C , CM000681.1:g.41512918T>C | GRCh37 |
| NC_000019.8:g.46204758T>C | NCBI36 |
| NG_007929.1:g.20715T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000324071.10:c.593T>C MANE Select | ENSP00000324648.2:p.Met198Thr | |
| ENST00000598834.2:c.495T>C | ||
| ENST00000324071.8:c.593T>C | ENSP00000324648.2:p.Met198Thr | |
| ENST00000593831.1:c.256+2567T>C | ENSP00000470582.1:n.256+2567T>C | |
| ENST00000594187.1:n.177T>C | ||
| ENST00000598834.1:n.495T>C | ||
| NM_000767.4:c.593T>C | NP_000758.1:p.Met198Thr | |
| XM_005258569.3:c.593T>C | XP_005258626.1:p.Met198Thr | |
| XM_006723050.2:c.593T>C | XP_006723113.1:p.Met198Thr | |
| XM_011526546.1:c.593T>C | XP_011524848.1:p.Met198Thr | |
| XM_011526547.1:c.593T>C | XP_011524849.1:p.Met198Thr | |
| XM_011526548.1:c.484+2567T>C | XP_011524850.1:n.484+2567T>C | |
| XM_011526549.1:c.2T>C | XP_011524851.1:p.Met1Thr | |
| XM_011526550.1:c.364+2567T>C | XP_011524852.1:n.364+2567T>C | |
| NM_000767.5:c.593T>C MANE Select | NP_000758.1:p.Met198Thr |