MyVariant.info:
GRCh37
chr5:g.156608012A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157181001A>G , CM000667.2:g.157181001A>G | GRCh38 |
| NC_000005.9:g.156608012A>G , CM000667.1:g.156608012A>G | GRCh37 |
| NC_000005.8:g.156540590A>G | NCBI36 |
| NG_016276.1:g.5106A>G , LRG_189:g.5106A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696962.1:c.24A>G | ENSP00000513001.1:p.Glu8= | |
| ENST00000422843.8:c.24A>G MANE Select | ENSP00000398655.4:p.Glu8= | |
| ENST00000422843.7:c.24A>G | ENSP00000398655.3:p.Glu8= | |
| ENST00000517779.1:c.24A>G | ENSP00000431054.1:p.Glu8= | |
| ENST00000519402.5:n.159A>G | ||
| ENST00000520555.5:n.162A>G | ||
| ENST00000521769.5:c.-238+14855A>G | ENSP00000430327.1:n.-238+14855A>G | |
| ENST00000522616.1:n.165A>G | ||
| NM_005546.3:c.24A>G , LRG_189t1:c.24A>G | NP_005537.3:p.Glu8= | |
| NM_005546.4:c.24A>G MANE Select | NP_005537.3:p.Glu8= |