MyVariant.info:
GRCh37
chr13:g.32968951C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32394814C>A , CM000675.2:g.32394814C>A | GRCh38 |
| NC_000013.10:g.32968951C>A , CM000675.1:g.32968951C>A | GRCh37 |
| NC_000013.9:g.31866951C>A | NCBI36 |
| NG_012772.3:g.84335C>A , LRG_293:g.84335C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000470094.2:c.9382C>A | ENSP00000434898.2:p.Arg3128= | |
| ENST00000528762.2:c.*749C>A | ENSP00000433168.2:n.*749C>A | |
| ENST00000530893.7:c.9013C>A | ENSP00000499438.2:p.Arg3005= | |
| ENST00000665585.2:c.*944C>A | ENSP00000499570.2:n.*944C>A | |
| ENST00000666593.2:c.*227C>A | ENSP00000499256.2:n.*227C>A | |
| ENST00000700202.2:c.9331C>A | ENSP00000514856.2:p.Arg3111= | |
| ENST00000700202.1:c.1798C>A | ENSP00000514856.1:p.Arg600= | |
| ENST00000700203.1:n.1509C>A | ||
| ENST00000380152.8:c.9382C>A MANE Select | ENSP00000369497.3:p.Arg3128= | |
| ENST00000544455.6:c.9382C>A | ENSP00000439902.1:p.Arg3128= | |
| ENST00000614259.2:c.9390C>A | ENSP00000506251.1:n.9390C>A | |
| ENST00000665585.1:c.2260C>A | ||
| ENST00000666593.1:c.404C>A | ENSP00000499256.1:n.404C>A | |
| ENST00000680887.1:c.9382C>A | ENSP00000505508.1:p.Arg3128= | |
| ENST00000380152.7:c.9382C>A | ENSP00000369497.3:p.Arg3128= | |
| ENST00000470094.1:c.339C>A | ||
| ENST00000544455.5:c.9382C>A | ENSP00000439902.1:p.Arg3128= | |
| NM_000059.3:c.9382C>A , LRG_293t1:c.9382C>A | NP_000050.2:p.Arg3128= | |
| XM_011535203.1:c.9382C>A | XP_011533505.1:p.Arg3128= | |
| XM_011535204.1:c.9286C>A | XP_011533506.1:p.Arg3096= | |
| NM_000059.4:c.9382C>A MANE Select | NP_000050.3:p.Arg3128= |