MyVariant.info:
GRCh37
chr17:g.7906632C>T
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8003314C>T , CM000679.2:g.8003314C>T | GRCh38 |
| NC_000017.10:g.7906632C>T , CM000679.1:g.7906632C>T | GRCh37 |
| NC_000017.9:g.7847357C>T | NCBI36 |
| NG_009092.1:g.5645C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254854.5:c.267C>T MANE Select | ENSP00000254854.4:p.Gly89= | |
| ENST00000254854.4:c.267C>T | ENSP00000254854.4:p.Gly89= | |
| NM_000180.3:c.267C>T | NP_000171.1:p.Gly89= | |
| XM_011523816.1:c.267C>T | XP_011522118.1:p.Gly89= | |
| NM_000180.4:c.267C>T MANE Select | NP_000171.1:p.Gly89= |