HGVS | Genome Assembly |
---|---|
NC_000006.12:g.52186411A= , CM000668.2:g.52186411A= | GRCh38 |
NC_000006.11:g.52051209A= , CM000668.1:g.52051209A= | GRCh37 |
NC_000006.10:g.52159168A= | NCBI36 |
NG_033021.1:g.5025A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000648244.1:c.-21A= MANE Select | ENSP00000497968.1:n.-21A= | |
ENST00000340057.1:c.-21A= | ENSP00000344192.1:n.-21A= | |
NM_002190.2:c.-21A= | NP_002181.1:n.-21A= | |
NM_002190.3:c.-21A= MANE Select | NP_002181.1:n.-21A= |