MyVariant.info:
GRCh37
chr2:g.39278375C>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39051234C>T , CM000664.2:g.39051234C>T | GRCh38 |
| NC_000002.11:g.39278375C>T , CM000664.1:g.39278375C>T | GRCh37 |
| NC_000002.10:g.39131879C>T | NCBI36 |
| NG_007530.1:g.74230G>A , LRG_754:g.74230G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461545.2:n.801G>A | ||
| ENST00000472480.2:n.654G>A | ||
| ENST00000685782.1:n.1612G>A | ||
| ENST00000689668.1:n.781G>A | ||
| ENST00000690679.1:c.874G>A | ||
| ENST00000690876.1:c.774G>A | ENSP00000508955.1:p.Lys258= | |
| ENST00000691229.1:c.774G>A | ENSP00000510437.1:p.Lys258= | |
| ENST00000692089.1:c.774G>A | ENSP00000508626.1:p.Lys258= | |
| ENST00000402219.8:c.774G>A MANE Select | ENSP00000384675.2:p.Lys258= | |
| ENST00000395038.6:c.774G>A | ENSP00000378479.2:p.Lys258= | |
| ENST00000402219.6:c.774G>A | ENSP00000384675.2:p.Lys258= | |
| ENST00000426016.5:c.774G>A | ENSP00000387784.1:p.Lys258= | |
| ENST00000461545.1:n.124G>A | ||
| NM_005633.3:c.774G>A , LRG_754t1:c.774G>A | NP_005624.2:p.Lys258= | |
| XM_005264515.3:c.774G>A | XP_005264572.1:p.Lys258= | |
| XM_011533060.1:c.867G>A | XP_011531362.1:p.Lys289= | |
| XM_011533061.1:c.867G>A | XP_011531363.1:p.Lys289= | |
| XM_011533062.1:c.753G>A | XP_011531364.1:p.Lys251= | |
| XM_011533063.1:c.750G>A | XP_011531365.1:p.Lys250= | |
| XM_011533064.1:c.603G>A | XP_011531366.1:p.Lys201= | |
| XM_011533065.1:c.867G>A | XP_011531367.1:p.Lys289= | |
| XM_005264515.4:c.774G>A | XP_005264572.1:p.Lys258= | |
| XM_011533062.2:c.753G>A | XP_011531364.1:p.Lys251= | |
| XM_011533064.2:c.603G>A | XP_011531366.1:p.Lys201= | |
| NM_001382394.1:c.753G>A | NP_001369323.1:p.Lys251= | |
| NM_001382395.1:c.774G>A | NP_001369324.1:p.Lys258= | |
| NM_005633.4:c.774G>A MANE Select | NP_005624.2:p.Lys258= |