MyVariant.info:
GRCh37
chr7:g.24329133C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.24289514C>A , CM000669.2:g.24289514C>A | GRCh38 |
| NC_000007.13:g.24329133C>A , CM000669.1:g.24329133C>A | GRCh37 |
| NC_000007.12:g.24295658C>A | NCBI36 |
| NG_016148.1:g.10327C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242152.7:c.204C>A MANE Select | ENSP00000242152.2:p.Ser68= | |
| ENST00000242152.6:c.204C>A | ENSP00000242152.2:p.Ser68= | |
| ENST00000405982.1:c.204C>A | ENSP00000385282.1:p.Ser68= | |
| ENST00000407573.5:c.204C>A | ENSP00000384364.1:p.Ser68= | |
| NM_000905.3:c.204C>A | NP_000896.1:p.Ser68= | |
| XM_017012910.1:c.41+29843G>T | XP_016868399.1:n.41+29843G>T | |
| XM_017012911.1:c.41+29843G>T | XP_016868400.1:n.41+29843G>T | |
| XR_001745121.1:n.473+29843G>T | ||
| XR_001745122.1:n.345-92485G>T | ||
| XR_001745123.1:n.473+29843G>T | ||
| XR_001745124.1:n.473+29843G>T | ||
| XR_001745125.1:n.473+29843G>T | ||
| XR_001745126.1:n.473+29843G>T | ||
| XR_001745127.1:n.345-33815G>T | ||
| XR_001745129.1:n.473+29843G>T | ||
| XR_001745130.1:n.473+29843G>T | ||
| XR_001745131.1:n.473+29843G>T | ||
| XR_001745132.1:n.473+29843G>T | ||
| NM_000905.4:c.204C>A MANE Select | NP_000896.1:p.Ser68= |