MyVariant.info:
GRCh37
chr11:g.72946020C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.73234975C>A , CM000673.2:g.73234975C>A | GRCh38 |
| NC_000011.9:g.72946020C>A , CM000673.1:g.72946020C>A | GRCh37 |
| NC_000011.8:g.72623668C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393597.7:c.816C>A MANE Select | ENSP00000377222.2:p.Arg272= | |
| ENST00000311131.6:c.816C>A | ENSP00000310305.2:p.Arg272= | |
| ENST00000393596.2:c.816C>A | ENSP00000377221.2:p.Arg272= | |
| ENST00000393597.6:c.816C>A | ENSP00000377222.2:p.Arg272= | |
| NM_002564.3:c.816C>A | NP_002555.3:p.Arg272= | |
| NM_176071.2:c.816C>A | NP_788085.2:p.Arg272= | |
| NM_176072.2:c.816C>A | NP_788086.2:p.Arg272= | |
| XM_005274019.3:c.816C>A | XP_005274076.1:p.Arg272= | |
| XM_005274020.3:c.816C>A | XP_005274077.1:p.Arg272= | |
| XM_005274021.3:c.816C>A | XP_005274078.1:p.Arg272= | |
| XM_011545074.1:c.816C>A | XP_011543376.1:p.Arg272= | |
| XM_005274019.4:c.816C>A | XP_005274076.1:p.Arg272= | |
| XM_005274020.4:c.816C>A | XP_005274077.1:p.Arg272= | |
| XM_005274021.4:c.816C>A | XP_005274078.1:p.Arg272= | |
| XM_011545074.2:c.816C>A | XP_011543376.1:p.Arg272= | |
| XM_017017839.1:c.816C>A | XP_016873328.1:p.Arg272= | |
| XR_001747890.1:n.1168C>A | ||
| XR_001747891.1:n.1168C>A | ||
| XR_001747892.1:n.1168C>A | ||
| NM_002564.4:c.816C>A MANE Select | NP_002555.4:p.Arg272= | |
| NM_176071.3:c.816C>A | NP_788085.3:p.Arg272= | |
| NM_176072.3:c.816C>A | NP_788086.3:p.Arg272= |