HGVS | Genome Assembly |
---|---|
NC_000019.10:g.49636358A= , CM000681.2:g.49636358A= | GRCh38 |
NC_000019.9:g.50139615A= , CM000681.1:g.50139615A= | GRCh37 |
NC_000019.8:g.54831427A= | NCBI36 |
NG_042222.1:g.8786T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000246792.4:c.453+261T= MANE Select | ENSP00000246792.2:n.453+261T= | |
ENST00000246792.3:c.453+261T= | ENSP00000246792.2:n.453+261T= | |
ENST00000601532.1:n.593+261T= | ||
NM_006270.3:c.453+261T= | NP_006261.1:n.453+261T= | |
NM_006270.4:c.453+261T= | NP_006261.1:n.453+261T= | |
NM_006270.5:c.453+261T= MANE Select | NP_006261.1:n.453+261T= |