Linked Data
ClinVar Variation Id:
2144637
ClinVar RCV Id:
RCV003071034
dbSNP Id:
rs199714091
ExAC:
16:17232375 G / A
gnomAD v2:
16-17232375-G-A
gnomAD v3:
16-17138518-G-A
gnomAD v4:
16-17138518-G-A
COSMIC:
COSM4058680
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.17138518G>A , CM000678.2:g.17138518G>A | GRCh38 |
| NC_000016.9:g.17232375G>A , CM000678.1:g.17232375G>A | GRCh37 |
| NC_000016.8:g.17139876G>A | NCBI36 |
| NG_015843.1:g.337364C>T | |
| NG_015843.2:g.337364C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261381.7:c.1601C>T MANE Select | ENSP00000261381.6:p.Thr534Met | |
| ENST00000261381.6:c.1601C>T | ENSP00000261381.6:p.Thr534Met | |
| NM_022166.3:c.1601C>T | NP_071449.1:p.Thr534Met | |
| XM_011522574.1:c.1601C>T | XP_011520876.1:p.Thr534Met | |
| XR_933141.1:n.451G>A | ||
| NR_135179.1:n.423G>A | ||
| XM_017023539.2:c.1601C>T | XP_016879028.1:p.Thr534Met | |
| XM_017023540.2:c.1601C>T | XP_016879029.1:p.Thr534Met | |
| NM_022166.4:c.1601C>T MANE Select | NP_071449.1:p.Thr534Met |