Linked Data
ClinVar Variation Id:
3064861
ClinVar RCV Id:
RCV003989938
dbSNP Id:
rs1415664013
gnomAD v4:
10-100989037-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.100989037C>T , CM000672.2:g.100989037C>T | GRCh38 |
| NC_000010.10:g.102748794C>T , CM000672.1:g.102748794C>T | GRCh37 |
| NC_000010.9:g.102738784C>T | NCBI36 |
| NG_011646.1:g.3479G>A | |
| NG_012624.1:g.6502C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311916.8:c.827C>T MANE Select | ENSP00000309595.2:p.Thr276Met | |
| ENST00000370228.2:c.827C>T | ENSP00000359248.1:p.Thr276Met | |
| ENST00000643860.1:c.827C>T | ENSP00000494389.1:p.Thr276Met | |
| ENST00000646226.1:n.59-607C>T | ||
| ENST00000311916.6:c.827C>T | ENSP00000309595.2:p.Thr276Met | |
| ENST00000370228.1:c.827C>T | ENSP00000359248.1:p.Thr276Met | |
| ENST00000459764.1:n.87-607C>T | ||
| ENST00000473656.5:n.65-607C>T | ||
| ENST00000476766.5:n.192-669C>T | ||
| NM_001163812.1:c.827C>T | NP_001157284.1:p.Thr276Met | |
| NM_001163813.1:c.-119-607C>T | NP_001157285.1:n.-119-607C>T | |
| NM_001163814.1:c.-119-607C>T | NP_001157286.1:n.-119-607C>T | |
| NM_021830.4:c.827C>T | NP_068602.2:p.Thr276Met | |
| XM_011539975.1:c.-57-669C>T | XP_011538277.1:n.-57-669C>T | |
| XR_945788.1:n.1660C>T | ||
| XM_011539975.2:c.-57-669C>T | XP_011538277.1:n.-57-669C>T | |
| XM_017016437.1:c.-474C>T | XP_016871926.1:n.-474C>T | |
| XR_001747142.1:n.1001C>T | ||
| XR_001747144.1:n.1001C>T | ||
| XR_002956991.1:n.1001C>T | ||
| XR_945788.2:n.1001C>T | ||
| NM_021830.5:c.827C>T MANE Select | NP_068602.2:p.Thr276Met | |
| NM_001163812.2:c.827C>T | NP_001157284.1:p.Thr276Met | |
| NM_001163813.2:c.-119-607C>T | NP_001157285.1:n.-119-607C>T | |
| NM_001163814.2:c.-119-607C>T | NP_001157286.1:n.-119-607C>T | |
| NM_001368275.1:c.-57-669C>T | NP_001355204.1:n.-57-669C>T | |
| NR_160738.1:n.1495C>T | ||
| NR_160739.1:n.72-607C>T | ||
| NR_160740.1:n.1495C>T | ||
| NR_160741.1:n.1495C>T | ||
| NR_160742.1:n.1495C>T |