Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134750555G= , CM000671.2:g.134750555G= | GRCh38 |
| NC_000009.11:g.137642401G= , CM000671.1:g.137642401G= | GRCh37 |
| NC_000009.10:g.136782222G= | NCBI36 |
| NG_008030.1:g.113750G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.1508G= | ENSP00000360885.4:p.Arg503= | |
| ENST00000371817.8:c.1508G= MANE Select | ENSP00000360882.3:p.Arg503= | |
| ENST00000371817.7:c.1508G= | ENSP00000360882.3:p.Arg503= | |
| ENST00000618395.4:c.1508G= | ENSP00000481360.1:p.Arg503= | |
| NM_000093.4:c.1508G= | NP_000084.3:p.Arg503= | |
| NM_001278074.1:c.1508G= | NP_001265003.1:p.Arg503= | |
| XR_929712.1:n.1910G= | ||
| XR_929713.1:n.1910G= | ||
| XM_017014266.2:c.1508G= | XP_016869755.1:p.Arg503= | |
| XR_001746183.1:n.1906G= | ||
| NM_000093.5:c.1508G= MANE Select | NP_000084.3:p.Arg503= |