Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.120811635C>T , CM000670.2:g.120811635C>T | GRCh38 |
| NC_000008.10:g.121823875C>T , CM000670.1:g.121823875C>T | GRCh37 |
| NC_000008.9:g.121893056C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_021021.4:c.209G>A MANE Select | NP_066301.1:p.Arg70Lys |
| ENST00000517992.2:c.209G>A MANE Select | ENSP00000431124.1:p.Arg70Lys |
| NM_021021.3:c.209G>A | NP_066301.1:p.Arg70Lys |
| ENST00000395601.7:c.209G>A | ENSP00000378965.3:p.Arg70Lys |
| ENST00000517992.1:c.209G>A | ENSP00000431124.1:p.Arg70Lys |
| ENST00000648490.1:c.209G>A | ENSP00000497707.1:p.Arg70Lys |
| XM_011517239.1:c.209G>A | XP_011515541.1:p.Arg70Lys |
| XM_011517239.2:c.209G>A | XP_011515541.1:p.Arg70Lys |