dbSNP:
MyVariant.info:
GRCh37
chr7:g.44579180G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44539581G>T , CM000669.2:g.44539581G>T | GRCh38 |
| NC_000007.13:g.44579180G>T , CM000669.1:g.44579180G>T | GRCh37 |
| NC_000007.12:g.44545705G>T | NCBI36 |
| NG_013088.1:g.6735C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381160.8:c.816C>A MANE Select | ENSP00000370552.3:p.Leu272= | |
| ENST00000289547.8:c.816C>A | ENSP00000289547.4:p.Leu272= | |
| ENST00000381160.7:c.816C>A | ENSP00000370552.3:p.Leu272= | |
| ENST00000423141.1:c.816C>A | ENSP00000404670.1:p.Leu272= | |
| ENST00000546276.5:c.816C>A | ENSP00000438033.1:p.Leu272= | |
| NM_001101648.1:c.816C>A | NP_001095118.1:p.Leu272= | |
| NM_001300967.1:c.816C>A | NP_001287896.1:p.Leu272= | |
| NM_013389.2:c.816C>A | NP_037521.2:p.Leu272= | |
| XM_011515326.1:c.816C>A | XP_011513628.1:p.Leu272= | |
| XM_011515327.1:c.816C>A | XP_011513629.1:p.Leu272= | |
| XM_011515326.3:c.816C>A | XP_011513628.1:p.Leu272= | |
| XM_011515328.2:c.-552C>A | XP_011513630.1:n.-552C>A | |
| XR_002956423.1:n.1208C>A | ||
| NM_001101648.2:c.816C>A MANE Select | NP_001095118.1:p.Leu272= | |
| NM_001300967.2:c.816C>A | NP_001287896.1:p.Leu272= | |
| NM_013389.3:c.816C>A | NP_037521.2:p.Leu272= |