MyVariant.info:
GRCh37
chr3:g.148916235T>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.149198448T>C , CM000665.2:g.149198448T>C | GRCh38 |
| NC_000003.11:g.148916235T>C , CM000665.1:g.148916235T>C | GRCh37 |
| NC_000003.10:g.150398925T>C | NCBI36 |
| NG_011800.3:g.28598A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264613.11:c.1632A>G MANE Select | ENSP00000264613.6:p.Glu544= | |
| ENST00000264613.10:c.1632A>G | ENSP00000264613.6:p.Glu544= | |
| ENST00000462336.5:n.6A>G | ||
| ENST00000471356.1:n.451A>G | ||
| ENST00000481169.5:c.1632A>G | ENSP00000418773.1:p.Glu544= | |
| ENST00000489736.5:n.857A>G | ||
| ENST00000490639.5:n.1664A>G | ||
| ENST00000494544.1:c.981A>G | ENSP00000420545.1:p.Glu327= | |
| ENST00000497797.5:n.241A>G | ||
| XM_006713499.2:c.1632A>G | XP_006713562.1:p.Glu544= | |
| XM_006713500.2:c.1632A>G | XP_006713563.1:p.Glu544= | |
| XM_006713501.2:c.1632A>G | XP_006713564.1:p.Glu544= | |
| XM_006713502.2:c.1632A>G | XP_006713565.1:p.Glu544= | |
| XM_011512435.1:c.1632A>G | XP_011510737.1:p.Glu544= | |
| XR_427361.2:n.1890A>G | ||
| XM_006713499.3:c.1632A>G | XP_006713562.1:p.Glu544= | |
| XM_006713500.4:c.1632A>G | XP_006713563.1:p.Glu544= | |
| XM_006713501.3:c.1632A>G | XP_006713564.1:p.Glu544= | |
| XM_011512435.2:c.1632A>G | XP_011510737.1:p.Glu544= | |
| XM_017005734.2:c.1632A>G | XP_016861223.1:p.Glu544= | |
| XM_017005735.2:c.1632A>G | XP_016861224.1:p.Glu544= | |
| XR_427361.3:n.1848A>G | ||
| NM_000096.4:c.1632A>G MANE Select | NP_000087.2:p.Glu544= | |
| NR_046371.2:n.1669A>G |