HGVS | Genome Assembly |
---|---|
NC_000022.11:g.39244798G= , CM000684.2:g.39244798G= | GRCh38 |
NC_000022.10:g.39640803G= , CM000684.1:g.39640803G= | GRCh37 |
NC_000022.9:g.37970749G= | NCBI36 |
NG_012111.1:g.5155C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331163.11:c.-835C= MANE Select | ENSP00000330382.6:n.-835C= | |
NM_002608.2:c.-835C= | NP_002599.1:n.-835C= | |
NM_002608.3:c.-835C= | NP_002599.1:n.-835C= | |
NM_002608.4:c.-835C= MANE Select | NP_002599.1:n.-835C= |