Linked Data
ClinVar Variation Id:
1798029
ClinVar RCV Id:
RCV002441843
MyVariant Identifiers:
chr16:g.2096213G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2046212G>A , CM000678.2:g.2046212G>A | GRCh38 |
| NC_000016.9:g.2096213G>A , CM000678.1:g.2096213G>A | GRCh37 |
| NC_000016.8:g.2036214G>A | NCBI36 |
| NG_005895.1:g.1907G>A , LRG_487:g.1907G>A | |
| NG_008412.1:g.6655C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651570.2:c.270C>T MANE Select | ENSP00000498421.1:p.Asn90= | |
| ENST00000651583.1:c.225C>T | ENSP00000498821.1:p.Asn75= | |
| ENST00000219066.5:c.294C>T | ENSP00000219066.1:p.Asn98= | |
| ENST00000561841.1:c.190C>T | ||
| ENST00000562120.1:n.3C>T | ||
| ENST00000566380.5:c.233C>T | ||
| ENST00000568513.5:c.173+68C>T | ||
| NM_002528.5:c.294C>T | NP_002519.1:p.Asn98= | |
| XM_011522505.1:c.294C>T | XP_011520807.1:p.Asn98= | |
| NM_001318193.1:c.294C>T | NP_001305122.1:p.Asn98= | |
| NM_001318194.1:c.24+68C>T | NP_001305123.1:n.24+68C>T | |
| NM_002528.6:c.294C>T | NP_002519.1:p.Asn98= | |
| XM_017023253.1:c.294C>T | XP_016878742.1:p.Asn98= | |
| NM_001318193.2:c.270C>T | NP_001305122.2:p.Asn90= | |
| NM_002528.7:c.270C>T MANE Select | NP_002519.2:p.Asn90= | |
| NM_001318194.2:c.24+68C>T | NP_001305123.1:n.24+68C>T |