Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165770217G= , CM000664.2:g.165770217G= | GRCh38 |
| NC_000002.11:g.166626727G= , CM000664.1:g.166626727G= | GRCh37 |
| NC_000002.10:g.166334973G= | NCBI36 |
| NG_012069.1:g.29077C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004482.4:c.484C= MANE Select | NP_004473.2:p.Arg162= |
| ENST00000392701.8:c.484C= MANE Select | ENSP00000376465.3:p.Arg162= |
| NM_004482.3:c.484C= | NP_004473.2:p.Arg162= |
| ENST00000392701.7:c.484C= | ENSP00000376465.3:p.Arg162= |
| ENST00000412248.5:c.484C= | ENSP00000412643.1:p.Arg162= |
| XM_005246449.1:c.484C= | XP_005246506.1:p.Arg162= |
| XM_006712402.2:c.484C= | XP_006712465.1:p.Arg162= |
| XM_011510929.1:c.484C= | XP_011509231.1:p.Arg162= |
| XM_017003770.1:c.484C= | XP_016859259.1:p.Arg162= |
| XR_002959253.1:n.825C= |